Product NDC: | 67871-111 |
Proprietary Name: | SUCRAID |
Non Proprietary Name: | sacrosidase |
Active Ingredient(s): | 8500 [iU]/mL & nbsp; sacrosidase |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67871-111 |
Labeler Name: | QOL Medical, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020772 |
Marketing Category: | NDA |
Start Marketing Date: | 19980409 |
Package NDC: | 67871-111-04 |
Package Description: | 2 BOTTLE in 1 CARTON (67871-111-04) > 118 mL in 1 BOTTLE (67871-111-01) |
NDC Code | 67871-111-04 |
Proprietary Name | SUCRAID |
Package Description | 2 BOTTLE in 1 CARTON (67871-111-04) > 118 mL in 1 BOTTLE (67871-111-01) |
Product NDC | 67871-111 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sacrosidase |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 19980409 |
Marketing Category Name | NDA |
Labeler Name | QOL Medical, LLC |
Substance Name | SACROSIDASE |
Strength Number | 8500 |
Strength Unit | [iU]/mL |
Pharmaceutical Classes | Sucrose-specific Enzyme [EPC] |