NDC 65862-036 – Lamivudine and Zidovudine
Lamivudine 150 mg/1; Zidovudine 300 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-036
Product details
- Brand name
- Lamivudine and Zidovudine
- Generic name
- Lamivudine and Zidovudine
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077558
- Marketed since
- May 5, 2017
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 65862-036-10 | 6 BLISTER PACK in 1 CARTON (65862-036-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK | May 5, 2017 |
| 65862-036-60 | 60 TABLET, FILM COATED in 1 BOTTLE (65862-036-60) | May 5, 2017 |
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