Doxycycline
NDC 70771-1008, Doxycycline, tablet, film coated, from Zydus Lifesciences Limited.
- Product NDC
- 70771-1008
- Status
- Listed
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209582
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1008 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DOXYCYCLINE100 mg/1
Pharmacologic classes
Tetracycline-class Drug [EPC]; Tetracyclines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70771-1008-7 | 70771100807 | 50 TABLET, FILM COATED in 1 BOTTLE (70771-1008-7) |
| 70771-1008-8 | 70771100808 | 250 TABLET, FILM COATED in 1 BOTTLE (70771-1008-8) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c886b2e4-494a-4325-abaf-981fc3d01c66
Use it
Look up 70771-1008 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1008 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70771-1008. 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.