NDC 70710-1366 – Emtricitabine and tenofovir disoproxil fumarate
Emtricitabine 167 mg/1; Tenofovir Disoproxil Fumarate 250 mg/1 · Tablet, Film Coated · Oral
Product NDC70710-1366
Product details
- Brand name
- Emtricitabine and tenofovir disoproxil fumarate
- Generic name
- Emtricitabine and tenofovir disoproxil fumarate
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA212689
- Marketed since
- July 1, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor; Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor; Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor
Active ingredients
- Emtricitabine 167 mg/1
- Tenofovir Disoproxil Fumarate 250 mg/1
Uses, dosage, side effects and warnings for Emtricitabine and tenofovir disoproxil fumarate →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70710-1366-3 | 30 TABLET, FILM COATED in 1 BOTTLE (70710-1366-3) | Jul 1, 2021 |
| 70710-1366-4 | 10 BLISTER PACK in 1 CARTON (70710-1366-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1366-2) | Jul 1, 2021 |
| 70710-1366-9 | 90 TABLET, FILM COATED in 1 BOTTLE (70710-1366-9) | Jul 1, 2021 |
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