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STAVUDINE
STAVUDINE - 49349-066-02 - (STAVUDINE)
Drug Information of STAVUDINE
| Product NDC: | 49349-066 |
| Proprietary Name: | STAVUDINE |
| Non Proprietary Name: | STAVUDINE |
| Active Ingredient(s): | 40 mg/1 & nbsp; STAVUDINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of STAVUDINE
| Product NDC: | 49349-066 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077672 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101111 |
Package Information of STAVUDINE
| Package NDC: | 49349-066-02 |
| Package Description: | 30 CAPSULE in 1 BLISTER PACK (49349-066-02) |
NDC Information of STAVUDINE
| NDC Code | 49349-066-02 |
| Proprietary Name | STAVUDINE |
| Package Description | 30 CAPSULE in 1 BLISTER PACK (49349-066-02) |
| Product NDC | 49349-066 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | STAVUDINE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20101111 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | STAVUDINE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
