Does CREEKWOOD PHARMS have other FDA approval records?

Yes. Argus HQ has recorded 3 total FDA actions tied to CREEKWOOD PHARMS, including 3 approval records.

MIRABEGRON (CREEKWOOD PHARMS): FDA ORIG Approval, Not disclosed in the FDA record.

Key facts

Sponsor	CREEKWOOD PHARMS
Brand name	MIRABEGRON
Generic name	unspecified
Dosage form	TABLET, EXTENDED RELEASE
Application number	ANDA219599
Submission number	1
Submission type	ORIG
Review priority	STANDARD
Status date	Not disclosed in the FDA record.

The short version: CREEKWOOD PHARMS received anda approval for MIRABEGRON (unspecified) on 2026-10-07. Application number ANDA219599, submission type ORIG (submission 1). Dosage form: TABLET, EXTENDED RELEASE. FDA publishes approval and submission records so physicians, competitors, and investors can track which sponsors and products have cleared a given regulatory pathway. An approval reflects FDA's determination on the application as submitted; any post-approval changes to manufacturing, labeling, or use typically require a separate supplemental submission. FDA publishes approval and submission records so physicians, competitors, and investors can track which sponsors and products have cleared a given regulatory pathway. An approval reflects FDA's determination on the application as submitted; any post-approval changes to manufacturing, labeling, or use typically require a separate supplemental submission.

Regulatory context

This application was reviewed under FDA's ORIG submission pathway. An Abbreviated New Drug Application (ANDA) is the FDA pathway used to approve generic drug products. Instead of repeating the clinical efficacy and safety trials already performed for the original branded product, an ANDA sponsor must demonstrate that its generic version is bioequivalent to an already-approved reference listed drug and meets the same identity, strength, quality, purity, and manufacturing standards. FDA approval of an application does not itself guarantee ongoing marketing; sponsors remain subject to post-approval manufacturing inspections and adverse-event reporting requirements. FDA publishes approval and submission records so physicians, competitors, and investors can track which sponsors and products have cleared a given regulatory pathway. An approval reflects FDA's determination on the application as submitted; any post-approval changes to manufacturing, labeling, or use typically require a separate supplemental submission.

What was approved

FDA's record shows CREEKWOOD PHARMS as the sponsor of MIRABEGRON, with the generic name recorded as unspecified and dosage form TABLET, EXTENDED RELEASE. An Abbreviated New Drug Application (ANDA) is the FDA pathway used to approve generic drug products. Instead of repeating the clinical efficacy and safety trials already performed for the original branded product, an ANDA sponsor must demonstrate that its generic version is bioequivalent to an already-approved reference listed drug and meets the same identity, strength, quality, purity, and manufacturing standards. This specific application is submission type ORIG (submission number 1) under application number ANDA219599, with a submission status date of 20261007. FDA publishes approval and submission records so physicians, competitors, and investors can track which sponsors and products have cleared a given regulatory pathway. An approval reflects FDA's determination on the application as submitted; any post-approval changes to manufacturing, labeling, or use typically require a separate supplemental submission. This record is drawn directly from FDA's own approvals database rather than from company press materials. FDA publishes approval and submission records so physicians, competitors, and investors can track which sponsors and products have cleared a given regulatory pathway. An approval reflects FDA's determination on the application as submitted; any post-approval changes to manufacturing, labeling, or use typically require a separate supplemental submission. FDA publishes approval and submission records so physicians, competitors, and investors can track which sponsors and products have cleared a given regulatory pathway. An approval reflects FDA's determination on the application as submitted; any post-approval changes to manufacturing, labeling, or use typically require a separate supplemental submission.

CREEKWOOD PHARMS’s FDA history

Argus HQ has recorded 3 total FDA actions tied to CREEKWOOD PHARMS: 0 warning letters, 0 recalls, 3 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

What did FDA approve?: FDA's record shows anda approval for MIRABEGRON (unspecified), dosage form TABLET, EXTENDED RELEASE, sponsored by CREEKWOOD PHARMS, under application number ANDA219599. FDA publishes approval and submission records so physicians, competitors, and investors can track which sponsors and products have cleared a given regulatory pathway. An approval reflects FDA's determination on the application as submitted; any post-approval changes to manufacturing, labeling, or use typically require a separate supplemental submission.
What does the submission type mean?: An Abbreviated New Drug Application (ANDA) is the FDA pathway used to approve generic drug products. Instead of repeating the clinical efficacy and safety trials already performed for the original branded product, an ANDA sponsor must demonstrate that its generic version is bioequivalent to an already-approved reference listed drug and meets the same identity, strength, quality, purity, and manufacturing standards.
Is this product available now?: FDA's record lists a submission status date of 20261007. Availability, pricing, and distribution details beyond the submission status date are Not disclosed in the FDA record. FDA publishes approval and submission records so physicians, competitors, and investors can track which sponsors and products have cleared a given regulatory pathway. An approval reflects FDA's determination on the application as submitted; any post-approval changes to manufacturing, labeling, or use typically require a separate supplemental submission.
Does CREEKWOOD PHARMS have other FDA approval records?: Yes. Argus HQ has recorded 3 total FDA actions tied to CREEKWOOD PHARMS, including 3 approval records.

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Full FDA history for CREEKWOOD PHARMS

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). MIRABEGRON (CREEKWOOD PHARMS): FDA ORIG Approval, Not disclosed in the FDA record.. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/approval/creekwood-pharms-anda219599-2026-10-07

MLA

"MIRABEGRON (CREEKWOOD PHARMS): FDA ORIG Approval, Not disclosed in the FDA record.." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/approval/creekwood-pharms-anda219599-2026-10-07.

Chicago

Argus HQ Research. "MIRABEGRON (CREEKWOOD PHARMS): FDA ORIG Approval, Not disclosed in the FDA record.." Digital Empire Holdings LLC. Accessed October 14, 2026. https://argushq.ai/approval/creekwood-pharms-anda219599-2026-10-07.

BibTeX

@misc{argushq_argushq_ai_approval_creekwood_pharms_anda219599_2026_10_07_2026,
  title = {MIRABEGRON (CREEKWOOD PHARMS): FDA ORIG Approval, Not disclosed in the FDA record.},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/approval/creekwood-pharms-anda219599-2026-10-07},
  note = {Accessed: October 14, 2026}
}

Source: FDA.gov — Approvals ↗