70518-3612 : Finasteride 5 mg Oral Tablet, Film Coated


NDC: 70518-3612
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Finasteride
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA076511
Rev. Date: 


NDC Package Codes:

  • 70518-3612-0: 30 POUCH IN 1 BOX (70518‑3612‑0) / 1 TABLET, FILM COATED IN 1 POUCH (70518‑3612‑1)

Active Ingredients:

  • Finasteride

Dosage Strength:

  • 5 mg

Pharmaceutical Classes:

  • 5-alpha Reductase Inhibitor [EPC]
  • 5-alpha Reductase Inhibitors [MoA]

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NDC QR Code

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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.