Minocycline hydrochloride
NDC 68382-317, Minocycline hydrochloride, capsule, from Zydus Pharmaceuticals USA Inc..
- Product NDC
- 68382-317
- Status
- Listed
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- CAPSULE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA063009
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68382-317 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MINOCYCLINE HYDROCHLORIDE75 mg/1
Pharmacologic classes
Decreased Prothrombin Activity [PE]; Tetracycline-class Drug [EPC]; Tetracyclines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68382-317-01 | 68382031701 | 100 CAPSULE in 1 BOTTLE (68382-317-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/25acb785-6838-4e62-9e86-ddc30b2b759aNADAC price for package 68382031701
GET /v1/drugs/nadac/68382031701
Use it
Look up 68382-317 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68382-317 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68382-317. 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.