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VITRASE
VITRASE - 24208-002-01 - (hyaluronidase, ovine)
Drug Information of VITRASE
| Product NDC: | 24208-002 |
| Proprietary Name: | VITRASE |
| Non Proprietary Name: | hyaluronidase, ovine |
| Active Ingredient(s): | 200 [USP'U]/mL & nbsp; hyaluronidase, ovine |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VITRASE
| Product NDC: | 24208-002 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021640 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050201 |
Package Information of VITRASE
| Package NDC: | 24208-002-01 |
| Package Description: | 6 VIAL, SINGLE-USE in 1 CARTON (24208-002-01) > 1.2 mL in 1 VIAL, SINGLE-USE |
NDC Information of VITRASE
| NDC Code | 24208-002-01 |
| Proprietary Name | VITRASE |
| Package Description | 6 VIAL, SINGLE-USE in 1 CARTON (24208-002-01) > 1.2 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 24208-002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hyaluronidase, ovine |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20050201 |
| Marketing Category Name | NDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | HYALURONIDASE, OVINE |
| Strength Number | 200 |
| Strength Unit | [USP'U]/mL |
| Pharmaceutical Classes | Endoglycosidase [EPC],Glycoside Hydrolases [Chemical/Ingredient] |
