Pill Identifier Oxycodone Hydrochloride - NDC 57664-371
Oxycodone Hydrochloride
Product Code 57664-371
Oxycodone Hydrochloride by Sun Pharmaceutical Industries, Inc. is a gray rou tablet about 6 mm in size, imprinted with 371. The product is a human prescription drug with active ingredient(s) oxycodone hydrochloride.
Oxycodone Hydrochloride
Active Ingredient(s): Oxycodone Hydrochloride
Inactive Ingredient(s):
- ANHYDROUS LACTOSE
- SILICON DIOXIDE
- MAGNESIUM STEARATE
- MICROCRYSTALLINE CELLULOSE
- STARCH, CORN
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- FD&C BLUE NO. 1
- FD&C BLUE NO. 2
- FD&C YELLOW NO. 6
- FD&C RED NO. 40
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet
- Gray (C48324)
DEA Schedule: CII
Product Packages
NDC Package Code | Package Description |
---|---|
57664-371-88 | 100 TABLET in 1 BOTTLE |
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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.