NDC 71335-0639 – LAMIVUDINE and ZIDOVUDINE
Lamivudine 150 mg/1; Zidovudine 300 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0639
Product details
- Brand name
- LAMIVUDINE and ZIDOVUDINE
- Generic name
- LAMIVUDINE and ZIDOVUDINE
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA079124
- Marketed since
- September 18, 2015
- 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
- Lamivudine 150 mg/1
- Zidovudine 300 mg/1
Uses, dosage, side effects and warnings for LAMIVUDINE and ZIDOVUDINE →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0639-1 | 6 TABLET, FILM COATED in 1 BOTTLE (71335-0639-1) | Apr 2, 2021 |
| 71335-0639-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0639-2) | Dec 27, 2021 |
| 71335-0639-3 | 4 TABLET, FILM COATED in 1 BOTTLE (71335-0639-3) | Dec 27, 2021 |
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