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HYLENEX Recombinant
HYLENEX Recombinant - 18657-102-10 - (Hyaluronidase (Human Recombinant))
Drug Information of HYLENEX Recombinant
| Product NDC: | 18657-102 |
| Proprietary Name: | HYLENEX Recombinant |
| Non Proprietary Name: | Hyaluronidase (Human Recombinant) |
| Active Ingredient(s): | 150 [USP'U]/mL & nbsp; Hyaluronidase (Human Recombinant) |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HYLENEX Recombinant
| Product NDC: | 18657-102 |
| Labeler Name: | Halozyme, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021859 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20051202 |
Package Information of HYLENEX Recombinant
| Package NDC: | 18657-102-10 |
| Package Description: | 10 BOX in 1 CARTON (18657-102-10) > 1 VIAL in 1 BOX (18657-102-02) > 1 mL in 1 VIAL (18657-102-01) |
NDC Information of HYLENEX Recombinant
| NDC Code | 18657-102-10 |
| Proprietary Name | HYLENEX Recombinant |
| Package Description | 10 BOX in 1 CARTON (18657-102-10) > 1 VIAL in 1 BOX (18657-102-02) > 1 mL in 1 VIAL (18657-102-01) |
| Product NDC | 18657-102 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hyaluronidase (Human Recombinant) |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20051202 |
| Marketing Category Name | NDA |
| Labeler Name | Halozyme, Inc. |
| Substance Name | HYALURONIDASE (HUMAN RECOMBINANT) |
| Strength Number | 150 |
| Strength Unit | [USP'U]/mL |
| Pharmaceutical Classes | Endoglycosidase [EPC],Glycoside Hydrolases [Chemical/Ingredient] |
