Pill Identifier Diltiazem Hydrochloride Extended Release - NDC 68682-372
Diltiazem Hydrochloride
Product Code 68682-372
Diltiazem Hydrochloride Extended Release by Oceanside Pharmaceuticals is a white capsule capsule extended release about 23 mm in size, imprinted with 420. The product is a human prescription drug with active ingredient(s) diltiazem hydrochloride.
Diltiazem Hydrochloride Extended Release
Active Ingredient(s): Diltiazem Hydrochloride
Inactive Ingredient(s):
- D&C Red No. 28
- Ethyl Acrylate and Methyl Methacrylate Copolymer (2:1
- 750000 MW)
- FD&C Blue No. 1
- FD&C Green No. 3
- FD&C Red No. 40
- ferrosoferric oxide
- magnesium stearate
- polysorbate 80
- sucrose stearate
- talc
- titanium dioxide
- GELATIN, UNSPECIFIED
- HYPROMELLOSE, UNSPECIFIED
- MICROCRYSTALLINE CELLULOSE
- POVIDONE, UNSPECIFIED
Image of Diltiazem Hydrochloride Extended Release capsule, extended release by Oceanside Pharmaceuticals
Oceanside Pharmaceuticals
Product Type: Human Prescription Drug
Dosage Form: Capsule, Extended Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
68682-372-90 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
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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.