Pill Identifier Erlotinib - NDC 63304-096
Erlotinib
Product Code 63304-096
Erlotinib by Sun Pharmaceutical Industries, Inc. is a white rou tablet film coated about 10 mm in size, imprinted with rl12. The product is a human prescription drug with active ingredient(s) erlotinib.
Erlotinib
Active Ingredient(s): Erlotinib
Inactive Ingredient(s):
- HYPROMELLOSE 2208 (100 MPA.S)
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- MICROCRYSTALLINE CELLULOSE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- SODIUM LAURYL SULFATE
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- TALC
- TITANIUM DIOXIDE
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
63304-096-11 | 3 BLISTER PACK in 1 CARTON > 10 TABLET, FILM COATED in 1 BLISTER PACK (63304-096-31) |
63304-096-30 | 30 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.