Emtricitabine and Tenofovir Disoproxil Fumarate
- Product NDC
- 71205-776
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Emtricitabine and Tenofovir Disoproxil Fumarate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA090513
- Marketing category
- ANDA
- Substance
- EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-776-03 | 3 TABLET, FILM COATED in 1 BOTTLE (71205-776-03) | 2024-10-04 | | No | Historical |
| 71205-776-07 | 7 TABLET, FILM COATED in 1 BOTTLE (71205-776-07) | 2023-03-15 | | No | Historical |
| 71205-776-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-776-30) | 2023-03-15 | | No | Historical |
| 71205-776-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-776-60) | 2023-03-15 | | No | Historical |
| 71205-776-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-776-90) | 2023-03-15 | | No | Historical |