BLUEBERRY (Allergy Laboratories, Inc.)


Welcome to the PulseAid listing for the BLUEBERRY 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: blue ridge blueberry
SUBSTANCE NAME: BLUE RIDGE BLUEBERRY
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


BLUEBERRY HUMAN PRESCRIPTION DRUG Details:

Item DescriptionBLUEBERRY from Allergy Laboratories, Inc.
LABELER NAME: Allergy Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1(g/20mL)
START MARKETING DATE: 1972-08-29
END MARKETING DATE: 0000-00-00
PRODUCT ID: 54575-354_dbe7bebd-e445-4e59-8302-e706b795fbde
PRODUCT NDC: 54575-354
APPLICATION NUMBER: BLA102192

Other BLUE RIDGE BLUEBERRY Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Allergy Laboratories, Inc.BLUEBERRY