NDC 16714-534 – Emtricitabine and tenofovir disoproxil fumarate
Emtricitabine 200 mg/1; Tenofovir Disoproxil Fumarate 300 mg/1 · Tablet, Film Coated · Oral
Product NDC16714-534
Product details
- Brand name
- Emtricitabine and tenofovir disoproxil fumarate
- Generic name
- Emtricitabine and tenofovir disoproxil fumarate
- Labeler
- NorthStar RxLLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203442
- Marketed since
- March 9, 2022
- 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 200 mg/1
- Tenofovir Disoproxil Fumarate 300 mg/1
Uses, dosage, side effects and warnings for Emtricitabine and tenofovir disoproxil fumarate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 16714-534-01 | 30 TABLET, FILM COATED in 1 BOTTLE (16714-534-01) | Mar 9, 2022 |
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