Emtricitabine and tenofovir disoproxil fumarate
- Product NDC
- 68071-3695
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Emtricitabine and tenofovir disoproxil fumarate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA203442
- Marketing category
- ANDA
- Substance
- EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3695-3 | 3 TABLET, FILM COATED in 1 BOTTLE (68071-3695-3) | 2024-10-04 | | No | Historical |