BLACKBERRY (Allergy Laboratories, Inc.)
Welcome to the PulseAid listing for the BLACKBERRY drug offered from Allergy Laboratories, Inc.. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Allergy Laboratories, Inc. |
NON-PROPRIETARY NAME: | blackberry |
SUBSTANCE NAME: | BLACKBERRY |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | PERCUTANEOUS; SUBCUTANEOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | BLA |
START MARKETING DATE: | 1972-08-29 |
END MARKETING DATE: | 0000-00-00 |
BLACKBERRY HUMAN PRESCRIPTION DRUG Details:
Item Description | BLACKBERRY from Allergy Laboratories, Inc. |
LABELER NAME: | Allergy Laboratories, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1(g/20mL) |
START MARKETING DATE: | 1972-08-29 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 54575-353_dbe7bebd-e445-4e59-8302-e706b795fbde |
PRODUCT NDC: | 54575-353 |
APPLICATION NUMBER: | BLA102192 |
Other BLACKBERRY Pharmaceutical Manufacturers / Labelers: