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BLACKBERRY
BLACKBERRY - 54575-353-50 - (blackberry)
Drug Information of BLACKBERRY
| Product NDC: | 54575-353 |
| Proprietary Name: | BLACKBERRY |
| Non Proprietary Name: | blackberry |
| Active Ingredient(s): | 1 g/20mL & nbsp; blackberry |
| Administration Route(s): | PERCUTANEOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BLACKBERRY
| Product NDC: | 54575-353 |
| Labeler Name: | Allergy Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA102192 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19720829 |
Package Information of BLACKBERRY
| Package NDC: | 54575-353-50 |
| Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (54575-353-50) |
NDC Information of BLACKBERRY
| NDC Code | 54575-353-50 |
| Proprietary Name | BLACKBERRY |
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (54575-353-50) |
| Product NDC | 54575-353 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | blackberry |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | PERCUTANEOUS; SUBCUTANEOUS |
| Start Marketing Date | 19720829 |
| Marketing Category Name | BLA |
| Labeler Name | Allergy Laboratories, Inc. |
| Substance Name | BLACKBERRY |
| Strength Number | 1 |
| Strength Unit | g/20mL |
| Pharmaceutical Classes |
