71205-900 : Darifenacin 7.5 mg 7.5 mg Oral Tablet, Extended Release


NDC: 71205-900
Labeler: Proficient Rx Lp
Product Type: Human Prescription Drug
Drug Name:  Darifenacin 7.5 mg
Dosage Form: Oral Tablet, Extended Release
Application #: ANDA209571
Rev. Date: 


NDC Package Codes:

  • 71205-900-00: 100 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71205‑900‑00)
  • 71205-900-11: 1000 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71205‑900‑11)
  • 71205-900-30: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71205‑900‑30)
  • 71205-900-55: 500 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71205‑900‑55)
  • 71205-900-60: 60 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71205‑900‑60)
  • 71205-900-72: 120 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71205‑900‑72)
  • 71205-900-90: 90 TABLET, EXTENDED RELEASE IN 1 BOTTLE (71205‑900‑90)

Active Ingredients:

  • Darifenacin Hydrobromide

Dosage Strength:

  • 7.5 mg

Pharmaceutical Classes:

  • Cholinergic Muscarinic Antagonist [EPC]
  • Cholinergic Muscarinic Antagonists [MoA]

Related Products:

Based on records with the same trade name.
  • 70700-182 Darifenacin 7.5 mg 7.5 mg Oral Tablet, Extended Release by Xiromed, LLC

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.