NDC 31722-739 – Lamivudine and Zidovudine
Lamivudine 150 mg/1; Zidovudine 300 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-739
Product details
- Brand name
- Lamivudine and Zidovudine
- Generic name
- Lamivudine and Zidovudine
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203259
- Marketed since
- February 6, 2014
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 31722-739-05 | 500 TABLET, FILM COATED in 1 BOTTLE (31722-739-05) | Feb 6, 2014 |
| 31722-739-31 | 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-739-31) | Feb 6, 2014 |
| 31722-739-60 | 60 TABLET, FILM COATED in 1 BOTTLE (31722-739-60) | Feb 6, 2014 |
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