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SUSTIVA
SUSTIVA - 0056-0510-30 - (efavirenz)
Drug Information of SUSTIVA
| Product NDC: | 0056-0510 |
| Proprietary Name: | SUSTIVA |
| Non Proprietary Name: | efavirenz |
| Active Ingredient(s): | 600 mg/1 & nbsp; efavirenz |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUSTIVA
| Product NDC: | 0056-0510 |
| Labeler Name: | Bristol-Myers Squibb Pharma Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021360 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020102 |
Package Information of SUSTIVA
| Package NDC: | 0056-0510-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (0056-0510-30) |
NDC Information of SUSTIVA
| NDC Code | 0056-0510-30 |
| Proprietary Name | SUSTIVA |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0056-0510-30) |
| Product NDC | 0056-0510 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | efavirenz |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20020102 |
| Marketing Category Name | NDA |
| Labeler Name | Bristol-Myers Squibb Pharma Company |
| Substance Name | EFAVIRENZ |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA] |
