Pill Identifier Diltiazem Hydrochloride - NDC 68682-709
Diltiazem Hydrochloride Extended-release Tablets
Product Code 68682-709
Diltiazem Hydrochloride by Oceanside Pharmaceuticals is a white oval tablet extended release about 19 mm in size, imprinted with b;420;mg. The product is a human prescription drug with active ingredient(s) diltiazem hydrochloride extended-release tablets.
Diltiazem Hydrochloride
Active Ingredient(s): Diltiazem Hydrochloride Extended-release Tablets
Inactive Ingredient(s):
- carnauba wax
- silicon dioxide
- croscarmellose sodium
- ethyl acrylate and methyl methacrylate copolymer (2:1
- 750000 mw)
- HYPROMELLOSE, UNSPECIFIED
- magnesium stearate
- MICROCRYSTALLINE CELLULOSE
- microcrystalline wax
- polydextrose
- POLYETHYLENE GLYCOL, UNSPECIFIED
- polysorbate 80
- POVIDONE, UNSPECIFIED
- sucrose stearate
- talc
- titanium dioxide
Oceanside Pharmaceuticals
Product Type: Human Prescription Drug
Dosage Form: Tablet, Extended Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
68682-709-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE |
68682-709-90 | 90 TABLET, 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.