minocycline hydrochloride
NDC 68382-552, minocycline hydrochloride, tablet, extended release, from Zydus Pharmaceuticals (USA) Inc..
- Product NDC
- 68382-552
- Status
- Listed
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- 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/68382-552 \ -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 |
|---|---|---|
| 68382-552-01 | 68382055201 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-552-01) |
| 68382-552-05 | 68382055205 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-552-05) |
| 68382-552-06 | 68382055206 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-552-06) |
| 68382-552-10 | 68382055210 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-552-10) |
| 68382-552-16 | 68382055216 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-552-16) |
| 68382-552-30 | 68382055230 | 10 BLISTER PACK in 1 CARTON (68382-552-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/85f082a5-bba1-4441-ba28-4b8ec9a537f2
Use it
Look up 68382-552 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68382-552 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68382-552. 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.