Minocin
NDC 70842-160, minocycline hydrochloride, injection, from Melinta Therapeutics, LLC.
- Product NDC
- 70842-160
- Status
- Listed
- Labeler
- Melinta Therapeutics, LLC
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA050444
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70842-160 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MINOCYCLINE HYDROCHLORIDE100 mg/1
Pharmacologic classes
Decreased Prothrombin Activity [PE]; Tetracycline-class Drug [EPC]; Tetracyclines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70842-160-10 | 70842016010 | 10 VIAL in 1 CARTON (70842-160-10) / 1 INJECTION in 1 VIAL (70842-160-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e415c323-8219-464b-9e3e-72c5a796cdaa
Use it
Look up 70842-160 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70842-160 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70842-160. 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.