| Product NDC: | 0004-0244 | 
| Proprietary Name: | Invirase | 
| Non Proprietary Name: | saquinavir mesylate | 
| Active Ingredient(s): | 500 mg/1 & nbsp; saquinavir mesylate | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET, FILM COATED | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0004-0244 | 
| Labeler Name: | Genentech, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA021785 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 20041217 | 
| Package NDC: | 0004-0244-51 | 
| Package Description: | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0004-0244-51) | 
| NDC Code | 0004-0244-51 | 
| Proprietary Name | Invirase | 
| Package Description | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0004-0244-51) | 
| Product NDC | 0004-0244 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | saquinavir mesylate | 
| Dosage Form Name | TABLET, FILM COATED | 
| Route Name | ORAL | 
| Start Marketing Date | 20041217 | 
| Marketing Category Name | NDA | 
| Labeler Name | Genentech, Inc. | 
| Substance Name | SAQUINAVIR MESYLATE | 
| Strength Number | 500 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | HIV Protease Inhibitors [MoA],Protease Inhibitor [EPC] |