31722-739 : Lamivudine and Zidovudine Oral Tablet, Film Coated
NDC: | 31722-739 |
Labeler: | Camber Pharmaceuticals, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Lamivudine and Zidovudine |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA203259 |
Rev. Date: |
Appearance:
Markings: | I;115 |
Shapes: |
Capsule |
Colors: |
White |
Size (mm): | 17 |
Segments: * | 2 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces. |
NDC Package Codes:
- 31722-739-05: 500 TABLET, FILM COATED IN 1 BOTTLE (31722‑739‑05)
- 31722-739-31: 100 TABLET, FILM COATED IN 1 BLISTER PACK (31722‑739‑31)
- 31722-739-60: 60 TABLET, FILM COATED IN 1 BOTTLE (31722‑739‑60)
Active Ingredients:
- Lamivudine
- Zidovudine
Dosage Strength:
- 150 mg
- 300 mg
Inactive Ingredients:
- Hypromelloses
- Magnesium Stearate
- Cellulose, Microcrystalline
- Polyethylene Glycols
- Polysorbate 80
- Sodium Starch Glycolate Type a Potato
- Titanium Dioxide
Pharmaceutical Classes:
- Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
- Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
- Nucleoside Analog [EXT]
- Nucleoside Reverse Transcriptase Inhibitors [MoA]
Related Products:
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NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.