Emtricitabine and Tenofovir Disoproxil Fumarate
- Product NDC
- 59651-167
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Emtricitabine and Tenofovir Disoproxil Fumarate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA211640
- Marketing category
- ANDA
- Substance
- EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 59651-167-30 | 30 TABLET, FILM COATED in 1 BOTTLE (59651-167-30) | 2023-03-09 | | No | Historical |