49288-0205 : Standardized Meadow Fescue Grass Pollen 100000 [bau]/Ml Intradermal; Subcutaneous Injection, Solution


NDC: 49288-0205
Labeler: Antigen Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name: Standardized Meadow Fescue Grass Pollen
Dosage Form: Intradermal; Subcutaneous Injection, Solution
Application #: BLA102227
Rev. Date: 


NDC Package Codes:

  • 49288-0205-2: 5 ML IN 1 VIAL, MULTI‑DOSE (49288‑0205‑2)
  • 49288-0205-3: 10 ML IN 1 VIAL, MULTI‑DOSE (49288‑0205‑3)
  • 49288-0205-4: 30 ML IN 1 VIAL, MULTI‑DOSE (49288‑0205‑4)
  • 49288-0205-5: 50 ML IN 1 VIAL, MULTI‑DOSE (49288‑0205‑5)

Active Ingredients:

  • Festuca Pratensis Pollen

Dosage Strength:

  • 100000 [BAU]/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 36987-2319 Standardized Meadow Fescue Grass Pollen 100000 [bau]/Ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 36987-2320 Standardized Meadow Fescue Grass Pollen 10000 [bau]/Ml Intradermal; Subcutaneous Injection, Solution by Nelco Laboratories, Inc.
  • 54575-092 Standardized Meadow Fescue Grass Pollen 100000 [bau]/Ml Percutaneous; Subcutaneous Injection, Solution by Allergy Laboratories, Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 49288-0205 QR Code

< Prev: 49288-0204Next: 49288-0206 >

Related Discussions:

pollen-eze hay fever tablets
can anyone please help, i had a severe reaction to pollen-eze hay fever tablets a few years ago, i want to know what the... 2 replies
Loss of voice due to pollen allergies
I have been on Betamax 875mg plus 125mg twice a day. How long will it take to cure the loss of voice due to allergies? #... 1 reply
rye pollen extract
Can I take finasteride and prostabrit [rye pollen extract] togther?...




Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.