Varenicline
NDC 71921-307, Varenicline Tartrate, kit, from Florida Pharmaceutical Products, LLC.
- Product NDC
- 71921-307
- Status
- Listed
- Labeler
- Florida Pharmaceutical Products, LLC
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA219106
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71921-307 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71921-307-51 | 71921030751 | 1 KIT in 1 CARTON (71921-307-51) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2b9c8b1e-6193-4d8e-9b50-6aca27294263NADAC price for package 71921030751
GET /v1/drugs/nadac/71921030751
Use it
Look up 71921-307 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71921-307 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71921-307. 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.