33261-833 : Finasteride 5 mg/1 Oral Tablet
| NDC: | 33261-833 |
| Labeler: | Aidarex Pharmaceuticals LLC |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Finasteride |
| Dosage Form: | Oral Tablet |
| Application #: | ANDA090061 |
| Rev. Date: |
Appearance:
| Markings: | H;37 |
| Shapes: |
Round |
| Colors: |
 Blue |
| Size (mm): | 6 |
| 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. | |
NDC Package Codes:
- 33261-833-90: 90 TABLET IN 1 BOTTLE, PLASTIC (33261‑833‑90)
Active Ingredients:
- Finasteride
Dosage Strength:
- 5 mg
Inactive Ingredients:
- Lactose Monohydrate
- Cellulose, Microcrystalline
- Starch, Corn
- Sodium Starch Glycolate Type a Potato
- Docusate Sodium
- Magnesium Stearate
- Fd&c Blue No. 2
- Hypromelloses
- Talc
- Titanium Dioxide
- Ferric Oxide Yellow
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.