Diltiazem Hydrochloride
NDC 68682-997, Diltiazem Hydrochloride, capsule, extended release, from OCEANSIDE PHARMACEUTICALS.
- Product NDC
- 68682-997
- Status
- Listed
- Labeler
- OCEANSIDE PHARMACEUTICALS
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075116
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68682-997 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DILTIAZEM HYDROCHLORIDE240 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA]; Calcium Channel Blocker [EPC]; Cytochrome P450 3A4 Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68682-997-98 | 68682099798 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68682-997-98) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/43892b97-449d-45bc-bb09-29d47c655d65
Use it
Look up 68682-997 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68682-997 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68682-997. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.