68071-4808 : Finasteride 1 mg Oral Tablet, Film Coated


NDC: 68071-4808
Labeler: Nucare Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Finasteride
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA203687
Rev. Date: 


Appearance:


Markings: J;81
Shapes:  Octagon (8 sides)
Colors:  White
Size (mm): 7
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

J 81: (65862-927) Finasteride 1 mg Oral Tablet, Film Coated by Nucare Pharmaceuticals, Inc.
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 68071-4808-3: 30 TABLET, FILM COATED IN 1 BOTTLE (68071‑4808‑3)

Active Ingredients:

  • Finasteride

Dosage Strength:

  • 1 mg

Inactive Ingredients:

  • Docusate Sodium
  • Hydroxypropyl Cellulose (1600000 Wamw)
  • Hypromellose 2910 (6 Mpa.s)
  • Lactose Monohydrate
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Starch, Corn
  • Sodium Starch Glycolate Type a Potato
  • Talc
  • Titanium Dioxide /

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
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NDC QR Code

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NDC 68071-4808 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.