NDC 71335-0639-2
LAMIVUDINE and ZIDOVUDINE 150 mg/1
LAMIVUDINE and ZIDOVUDINE · TABLET, FILM COATED
LAMIVUDINE and ZIDOVUDINE is a tablet, film coated containing lamivudine and zidovudine at a strength of 150 mg/1. Manufactured by Bryant Ranch Prepack.
Key Facts
- Brand Name
- LAMIVUDINE and ZIDOVUDINE
- Generic Name
- LAMIVUDINE and ZIDOVUDINE
- NDC Code (Package)
71335-0639-2- NDC Code (Product)
71335-0639- Manufacturer
- Bryant Ranch Prepack
- Strength
- 150 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA079124
- Drug Class
- Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]; Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
- Marketing Start
- 09/18/2015
Recall History
No Recall HistoryView Full Drug Page
LAMIVUDINE and ZIDOVUDINE — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.