71335-0281 : Finasteride 1 mg Oral Tablet, Film Coated
NDC: | 71335-0281 |
Labeler: | Bryant Ranch Prepack |
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. |
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:
- 71335-0281-1: 30 TABLET, FILM COATED IN 1 BOTTLE (71335‑0281‑1)
- 71335-0281-2: 90 TABLET, FILM COATED IN 1 BOTTLE (71335‑0281‑2)
- 71335-0281-3: 60 TABLET, FILM COATED IN 1 BOTTLE (71335‑0281‑3)
- 71335-0281-4: 28 TABLET, FILM COATED IN 1 BOTTLE (71335‑0281‑4)
- 71335-0281-5: 180 TABLET, FILM COATED IN 1 BOTTLE (71335‑0281‑5)
Active Ingredients:
- Finasteride
Dosage Strength:
- 1 mg
Inactive Ingredients:
- Docusate Sodium
- Hydroxypropyl Cellulose (1200000 Mw)
- 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]
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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.