Diltiazem Hydrochloride
NDC 68071-4242, Diltiazem Hydrochloride, tablet, from NuCare Pharmaceuticals,Inc..
- Product NDC
- 68071-4242
- Status
- Listed
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA018602
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68071-4242 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DILTIAZEM HYDROCHLORIDE120 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA]; Calcium Channel Blocker [EPC]; Cytochrome P450 3A4 Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68071-4242-3 | 68071424203 | 30 TABLET in 1 BOTTLE (68071-4242-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/636556f6-2987-984f-e053-2991aa0a201a
Use it
Look up 68071-4242 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68071-4242 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68071-4242. 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.