Pill Identifier Methylphenidate Hydrochloride - NDC 57664-608
Methylphenidate Hydrochloride
Product Code 57664-608
Methylphenidate Hydrochloride by Sun Pharmaceutical Industries, Inc. is a white oval tablet extended release about 13 mm in size, imprinted with 36. The product is a human prescription drug with active ingredient(s) methylphenidate hydrochloride.
Methylphenidate Hydrochloride
Active Ingredient(s): Methylphenidate Hydrochloride
Inactive Ingredient(s):
- FERROSOFERRIC OXIDE
- CELLULOSE ACETATE
- SILICON DIOXIDE
- FD&C RED NO. 40
- FD&C BLUE NO. 2
- HYPROMELLOSE 2910 (6 MPA.S)
- PHOSPHORIC ACID
- POLOXAMER 188
- POLYETHYLENE OXIDE 200000
- POVIDONE K30
- PROPYLENE GLYCOL
- SHELLAC
- SODIUM CHLORIDE
- STEARIC ACID
- SUCCINIC ACID
- TITANIUM DIOXIDE
- TALC
- TRIACETIN
- FERRIC OXIDE YELLOW
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Extended Release
- White (C48325)
DEA Schedule: CII
Product Packages
NDC Package Code | Package Description |
---|---|
57664-608-88 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
* 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.