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Zidovudine
Zidovudine - 65862-048-24 - (Zidovudine)
Drug Information of Zidovudine
| Product NDC: | 65862-048 |
| Proprietary Name: | Zidovudine |
| Non Proprietary Name: | Zidovudine |
| Active Ingredient(s): | 10 mg/mL & nbsp; Zidovudine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zidovudine
| Product NDC: | 65862-048 |
| Labeler Name: | Aurobindo Pharma Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077268 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050919 |
Package Information of Zidovudine
| Package NDC: | 65862-048-24 |
| Package Description: | 240 mL in 1 BOTTLE (65862-048-24) |
NDC Information of Zidovudine
| NDC Code | 65862-048-24 |
| Proprietary Name | Zidovudine |
| Package Description | 240 mL in 1 BOTTLE (65862-048-24) |
| Product NDC | 65862-048 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Zidovudine |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20050919 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | ZIDOVUDINE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
