Product NDC: | 66593-3126 |
Proprietary Name: | Vancocin |
Non Proprietary Name: | vancomycin hydrochloride |
Active Ingredient(s): | 250 mg/1 & nbsp; vancomycin hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66593-3126 |
Labeler Name: | ViroPharma |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050606 |
Marketing Category: | NDA |
Start Marketing Date: | 19860415 |
Package NDC: | 66593-3126-2 |
Package Description: | 2 BLISTER PACK in 1 BOX (66593-3126-2) > 10 CAPSULE in 1 BLISTER PACK |
NDC Code | 66593-3126-2 |
Proprietary Name | Vancocin |
Package Description | 2 BLISTER PACK in 1 BOX (66593-3126-2) > 10 CAPSULE in 1 BLISTER PACK |
Product NDC | 66593-3126 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | vancomycin hydrochloride |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 19860415 |
Marketing Category Name | NDA |
Labeler Name | ViroPharma |
Substance Name | VANCOMYCIN HYDROCHLORIDE |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient] |