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ORRIS
ORRIS - 0268-0642-50 - (ORRIS)
Drug Information of ORRIS
| Product NDC: | 0268-0642 |
| Proprietary Name: | ORRIS |
| Non Proprietary Name: | ORRIS |
| Active Ingredient(s): | .05 g/mL & nbsp; ORRIS |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ORRIS
| Product NDC: | 0268-0642 |
| Labeler Name: | ALK-Abello, Inc. |
| Product Type: | NON-STANDARDIZED ALLERGENIC |
| FDA Application Number: | BLA103753 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19650101 |
Package Information of ORRIS
| Package NDC: | 0268-0642-50 |
| Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (0268-0642-50) |
NDC Information of ORRIS
| NDC Code | 0268-0642-50 |
| Proprietary Name | ORRIS |
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (0268-0642-50) |
| Product NDC | 0268-0642 |
| Product Type Name | NON-STANDARDIZED ALLERGENIC |
| Non Proprietary Name | ORRIS |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 19650101 |
| Marketing Category Name | BLA |
| Labeler Name | ALK-Abello, Inc. |
| Substance Name | ORRIS |
| Strength Number | .05 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
