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UPLAND SUMAC POLLEN - 54575-968-02 - (rhus glabra pollen)

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Drug Information of UPLAND SUMAC POLLEN

Product NDC: 54575-968
Proprietary Name: UPLAND SUMAC POLLEN
Non Proprietary Name: rhus glabra pollen
Active Ingredient(s): 1    g/20mL & nbsp;   rhus glabra pollen
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of UPLAND SUMAC POLLEN

Product NDC: 54575-968
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of UPLAND SUMAC POLLEN

Package NDC: 54575-968-02
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (54575-968-02)

NDC Information of UPLAND SUMAC POLLEN

NDC Code 54575-968-02
Proprietary Name UPLAND SUMAC POLLEN
Package Description 2 mL in 1 VIAL, MULTI-DOSE (54575-968-02)
Product NDC 54575-968
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rhus glabra pollen
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name RHUS GLABRA POLLEN
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes

Complete Information of UPLAND SUMAC POLLEN


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