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Zidovudine
Zidovudine - 48792-7809-6 - (Zidovudine)
Drug Information of Zidovudine
| Product NDC: | 48792-7809 |
| Proprietary Name: | Zidovudine |
| Non Proprietary Name: | Zidovudine |
| Active Ingredient(s): | 300 mg/1 & nbsp; Zidovudine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zidovudine
| Product NDC: | 48792-7809 |
| Labeler Name: | Sunshine Lake Pharma Co., Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202058 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120901 |
Package Information of Zidovudine
| Package NDC: | 48792-7809-6 |
| Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7809-6) |
NDC Information of Zidovudine
| NDC Code | 48792-7809-6 |
| Proprietary Name | Zidovudine |
| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7809-6) |
| Product NDC | 48792-7809 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Zidovudine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120901 |
| Marketing Category Name | ANDA |
| Labeler Name | Sunshine Lake Pharma Co., Ltd. |
| Substance Name | ZIDOVUDINE |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
