NDC 54575-087

STANDARDIZED KENTUCKY BLUEGRASS POLLEN

Poa Pratensis Pollen

STANDARDIZED KENTUCKY BLUEGRASS POLLEN is a Percutaneous; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Allergy Laboratories, Inc.. The primary component is Poa Pratensis Pollen.

Product ID54575-087_a3c0a62e-9b1b-41bf-9f8c-c0b58e36395c
NDC54575-087
Product TypeHuman Prescription Drug
Proprietary NameSTANDARDIZED KENTUCKY BLUEGRASS POLLEN
Generic NamePoa Pratensis Pollen
Dosage FormInjection, Solution
Route of AdministrationPERCUTANEOUS; SUBCUTANEOUS
Marketing Start Date1997-05-29
Marketing CategoryBLA / BLA
Application NumberBLA101380
Labeler NameAllergy Laboratories, Inc.
Substance NamePOA PRATENSIS POLLEN
Active Ingredient Strength100000 [BAU]/mL
Pharm ClassesStandardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 54575-087-10

10 mL in 1 VIAL, MULTI-DOSE (54575-087-10)
Marketing Start Date1997-05-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 54575-087-50 [54575008750]

STANDARDIZED KENTUCKY BLUEGRASS POLLEN INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA101380
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-05-29
Inactivation Date2020-01-31

NDC 54575-087-30 [54575008730]

STANDARDIZED KENTUCKY BLUEGRASS POLLEN INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA101380
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-05-29
Inactivation Date2020-01-31

NDC 54575-087-02 [54575008702]

STANDARDIZED KENTUCKY BLUEGRASS POLLEN INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA101380
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-05-29
Inactivation Date2020-01-31

NDC 54575-087-10 [54575008710]

STANDARDIZED KENTUCKY BLUEGRASS POLLEN INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA101380
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-05-29
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
POA PRATENSIS POLLEN100000 [BAU]/mL

Pharmacological Class

  • Standardized Pollen Allergenic Extract [EPC]
  • Increased Histamine Release [PE]
  • Cell-mediated Immunity [PE]
  • Increased IgG Production [PE]
  • Pollen [CS]
  • Allergens [CS]

NDC Crossover Matching brand name "STANDARDIZED KENTUCKY BLUEGRASS POLLEN" or generic name "Poa Pratensis Pollen"

NDCBrand NameGeneric Name
54575-087STANDARDIZED KENTUCKY BLUEGRASS POLLENPoa pratensis pollen
0268-0090CENTER-AL - POA PRATENSIS POLLENPOA PRATENSIS POLLEN
0268-0091CENTER-AL - POA PRATENSIS POLLENPOA PRATENSIS POLLEN
0268-0165CENTER-AL - POA PRATENSIS POLLENPOA PRATENSIS POLLEN

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