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CRIXIVAN
CRIXIVAN - 53808-0661-1 - (indinavir sulfate)
Drug Information of CRIXIVAN
| Product NDC: | 53808-0661 |
| Proprietary Name: | CRIXIVAN |
| Non Proprietary Name: | indinavir sulfate |
| Active Ingredient(s): | 400 mg/1 & nbsp; indinavir sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CRIXIVAN
| Product NDC: | 53808-0661 |
| Labeler Name: | State of Florida DOH Central Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020685 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090701 |
Package Information of CRIXIVAN
| Package NDC: | 53808-0661-1 |
| Package Description: | 30 CAPSULE in 1 BLISTER PACK (53808-0661-1) |
NDC Information of CRIXIVAN
| NDC Code | 53808-0661-1 |
| Proprietary Name | CRIXIVAN |
| Package Description | 30 CAPSULE in 1 BLISTER PACK (53808-0661-1) |
| Product NDC | 53808-0661 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | indinavir sulfate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | NDA |
| Labeler Name | State of Florida DOH Central Pharmacy |
| Substance Name | INDINAVIR SULFATE |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
