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Lamivudine and Zidovudine
Lamivudine and Zidovudine - 21695-996-02 - (Lamivudine and Zidovudine)
Drug Information of Lamivudine and Zidovudine
| Product NDC: | 21695-996 |
| Proprietary Name: | Lamivudine and Zidovudine |
| Non Proprietary Name: | Lamivudine and Zidovudine |
| Active Ingredient(s): | 150; 300 mg/1; mg/1 & nbsp; Lamivudine and Zidovudine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lamivudine and Zidovudine
| Product NDC: | 21695-996 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079081 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111227 |
Package Information of Lamivudine and Zidovudine
| Package NDC: | 21695-996-02 |
| Package Description: | 2 TABLET, FILM COATED in 1 BOTTLE (21695-996-02) |
NDC Information of Lamivudine and Zidovudine
| NDC Code | 21695-996-02 |
| Proprietary Name | Lamivudine and Zidovudine |
| Package Description | 2 TABLET, FILM COATED in 1 BOTTLE (21695-996-02) |
| Product NDC | 21695-996 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lamivudine and Zidovudine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111227 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | LAMIVUDINE; ZIDOVUDINE |
| Strength Number | 150; 300 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
