Pill Identifier Finasteride - NDC 47335-715
Product Code 47335-715
Finasteride by Sun Pharmaceutical Industries, Inc. is a blue rou about 7 mm in size, imprinted with 715. The product is a with active ingredient(s) .
Finasteride
Active Ingredient(s):
Inactive Ingredient(s):
- LACTOSE MONOHYDRATE
- STARCH, CORN
- CELLULOSE, MICROCRYSTALLINE
- POVIDONE K30
- DOCUSATE SODIUM
- TALC
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- MAGNESIUM STEARATE
- HYPROMELLOSE 2910 (15 MPA.S)
- POLYETHYLENE GLYCOL 6000
- TITANIUM DIOXIDE
- FD&C BLUE NO. 2
Sun Pharmaceutical Industries, Inc.
Product Type:
Dosage Form:
- Blue (C48333)
Product Packages
| NDC Package Code | Package Description |
|---|---|
| 47335-715-08 | 100 TABLET, FILM COATED in 1 BOTTLE |
| 47335-715-13 | 500 TABLET, FILM COATED in 1 BOTTLE |
| 47335-715-18 | 1000 TABLET, FILM COATED in 1 BOTTLE |
| 47335-715-81 | 90 TABLET, FILM COATED in 1 BOTTLE |
| 47335-715-83 | 30 TABLET, FILM COATED in 1 BOTTLE |
| 47335-715-88 | 100 TABLET, FILM COATED in 1 BOTTLE |
* Please review the disclaimer below.
Pill Identification data last updated on: December, 2018
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product. If this is an emergency, call 911 or the national Poison Help hotline at 1-800-222-1222. Most images are not part of the product labels and have not been verified by the labeler company. ALWAYS consult your physician or pharmacist with any medication-related questions.