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Stavudine
Stavudine - 64376-133-02 - (Stavudine)
Drug Information of Stavudine
| Product NDC: | 64376-133 |
| Proprietary Name: | Stavudine |
| Non Proprietary Name: | Stavudine |
| Active Ingredient(s): | 1 mg/mL & nbsp; Stavudine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Stavudine
| Product NDC: | 64376-133 |
| Labeler Name: | Boca Pharmacal Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078030 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120817 |
Package Information of Stavudine
| Package NDC: | 64376-133-02 |
| Package Description: | 200 mL in 1 BOTTLE (64376-133-02) |
NDC Information of Stavudine
| NDC Code | 64376-133-02 |
| Proprietary Name | Stavudine |
| Package Description | 200 mL in 1 BOTTLE (64376-133-02) |
| Product NDC | 64376-133 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Stavudine |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20120817 |
| Marketing Category Name | ANDA |
| Labeler Name | Boca Pharmacal Inc. |
| Substance Name | STAVUDINE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
