NDC 71335-1916 – Lamivudine and Zidovudine
Lamivudine 150 mg/1; Zidovudine 300 mg/1 · Tablet · Oral
Product NDC71335-1916
Product details
- Brand name
- Lamivudine and Zidovudine
- Generic name
- Lamivudine and Zidovudine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA090679
- Marketed since
- August 30, 2018
- 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 |
|---|---|---|
| 71335-1916-1 | 6 TABLET in 1 BOTTLE (71335-1916-1) | Jul 15, 2021 |
| 71335-1916-2 | 60 TABLET in 1 BOTTLE (71335-1916-2) | Apr 5, 2024 |
| 71335-1916-3 | 4 TABLET in 1 BOTTLE (71335-1916-3) | Apr 5, 2024 |
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