Pill Identifier Diltiazem Hydrochloride - NDC 63304-719
Diltiazem Hydrochloride
Product Code 63304-719
Diltiazem Hydrochloride by Sun Pharmaceutical Industries, Inc. is a blue capsule capsule extended release about 19 mm in size, imprinted with rg84. The product is a human prescription drug with active ingredient(s) diltiazem hydrochloride.
Diltiazem Hydrochloride
Active Ingredient(s): Diltiazem Hydrochloride
Inactive Ingredient(s):
- AMMONIO METHACRYLATE COPOLYMER TYPE B
- HYPROMELLOSE, UNSPECIFIED
- SODIUM LAURYL SULFATE
- TALC
- FD&C BLUE NO. 1
- GELATIN, UNSPECIFIED
- TITANIUM DIOXIDE
- FERROSOFERRIC OXIDE
- PROPYLENE GLYCOL
- POTASSIUM HYDROXIDE
- SHELLAC
- SUCROSE
- STARCH, CORN
- ACETYLTRIBUTYL CITRATE
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Capsule, Extended Release
- Blue (C48333)
Product Packages
NDC Package Code | Package Description |
---|---|
63304-719-05 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE |
63304-719-30 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE |
63304-719-90 | 90 CAPSULE, EXTENDED RELEASE 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.