minocycline hydrochloride
NDC 70771-1157, minocycline hydrochloride, tablet, extended release, from Zydus Lifesciences Limited.
- Product NDC
- 70771-1157
- Status
- Listed
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA203553
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1157 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MINOCYCLINE HYDROCHLORIDE105 mg/1
Pharmacologic classes
Decreased Prothrombin Activity [PE]; Tetracycline-class Drug [EPC]; Tetracyclines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70771-1157-0 | 70771115700 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1157-0) |
| 70771-1157-1 | 70771115701 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1157-1) |
| 70771-1157-3 | 70771115703 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1157-3) |
| 70771-1157-5 | 70771115705 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1157-5) |
| 70771-1157-7 | 70771115707 | 10 BLISTER PACK in 1 CARTON (70771-1157-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| 70771-1157-9 | 70771115709 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1157-9) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/8bf9cf23-8ffc-401f-981d-4878d694a468
Use it
Look up 70771-1157 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1157 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70771-1157. 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.