Home
>
National Drug Code (NDC)
>
BLUEBERRY
BLUEBERRY - 54575-354-50 - (blue ridge blueberry)
Drug Information of BLUEBERRY
| Product NDC: | 54575-354 |
| Proprietary Name: | BLUEBERRY |
| Non Proprietary Name: | blue ridge blueberry |
| Active Ingredient(s): | 1 g/20mL & nbsp; blue ridge blueberry |
| Administration Route(s): | PERCUTANEOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BLUEBERRY
| Product NDC: | 54575-354 |
| Labeler Name: | Allergy Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA102192 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19720829 |
Package Information of BLUEBERRY
| Package NDC: | 54575-354-50 |
| Package Description: | 50 mL in 1 VIAL, MULTI-DOSE (54575-354-50) |
NDC Information of BLUEBERRY
| NDC Code | 54575-354-50 |
| Proprietary Name | BLUEBERRY |
| Package Description | 50 mL in 1 VIAL, MULTI-DOSE (54575-354-50) |
| Product NDC | 54575-354 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | blue ridge blueberry |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | PERCUTANEOUS; SUBCUTANEOUS |
| Start Marketing Date | 19720829 |
| Marketing Category Name | BLA |
| Labeler Name | Allergy Laboratories, Inc. |
| Substance Name | BLUE RIDGE BLUEBERRY |
| Strength Number | 1 |
| Strength Unit | g/20mL |
| Pharmaceutical Classes |
