Product NDC: | 0548-9090 |
Proprietary Name: | AMPHADASE |
Non Proprietary Name: | hyaluronidase |
Active Ingredient(s): | 150 [USP'U]/mL & nbsp; hyaluronidase |
Administration Route(s): | SUBCUTANEOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0548-9090 |
Labeler Name: | Amphastar Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021665 |
Marketing Category: | NDA |
Start Marketing Date: | 20041026 |
Package NDC: | 0548-9090-10 |
Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0548-9090-10) > 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 0548-9090-10 |
Proprietary Name | AMPHADASE |
Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0548-9090-10) > 1 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 0548-9090 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | hyaluronidase |
Dosage Form Name | INJECTION |
Route Name | SUBCUTANEOUS |
Start Marketing Date | 20041026 |
Marketing Category Name | NDA |
Labeler Name | Amphastar Pharmaceuticals, Inc. |
Substance Name | HYALURONIDASE |
Strength Number | 150 |
Strength Unit | [USP'U]/mL |
Pharmaceutical Classes | Endoglycosidase [EPC],Glycoside Hydrolases [Chemical/Ingredient] |