Pill Identifier Oxcarbazepine - NDC 62756-184
Oxcarbazepine
Product Code 62756-184
Oxcarbazepine by Sun Pharmaceutical Industries, Inc. is a yellow capsule tablet film coated about 15 mm in size, imprinted with 184. The product is a human prescription drug with active ingredient(s) oxcarbazepine.
Oxcarbazepine
Active Ingredient(s): Oxcarbazepine
Inactive Ingredient(s):
- SILICON DIOXIDE
- POVIDONE K30
- POLYETHYLENE GLYCOL, UNSPECIFIED
- CROSCARMELLOSE SODIUM
- CROSPOVIDONE (15 MPA.S AT 5%)
- MICROCRYSTALLINE CELLULOSE
- SODIUM STEARYL FUMARATE
- HYPROMELLOSE, UNSPECIFIED
- TITANIUM DIOXIDE
- FERRIC OXIDE YELLOW
- POLYSORBATE 80
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
62756-184-08 | 100 TABLET, FILM COATED in 1 BOTTLE |
62756-184-13 | 500 TABLET, FILM COATED in 1 BOTTLE |
62756-184-18 | 1000 TABLET, FILM COATED in 1 BOTTLE |
62756-184-83 | 30 TABLET, FILM COATED in 1 BOTTLE |
62756-184-88 | 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.