NDC 22840-2464

Velvet Mesquite Pollen

Prosopis Velutina

Velvet Mesquite Pollen is a Intradermal; Percutaneous; Subcutaneous Solution in the Non-standardized Allergenic category. It is labeled and distributed by Greer Laboratories, Inc.. The primary component is Prosopis Velutina Seed.

Product ID22840-2464_83d281e9-375b-7e6c-e053-2991aa0a6f0e
NDC22840-2464
Product TypeNon-standardized Allergenic
Proprietary NameVelvet Mesquite Pollen
Generic NameProsopis Velutina
Dosage FormSolution
Route of AdministrationINTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS
Marketing Start Date1981-09-15
Marketing CategoryBLA / BLA
Application NumberBLA101833
Labeler NameGreer Laboratories, Inc.
Substance NamePROSOPIS VELUTINA SEED
Active Ingredient Strength0 g/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 22840-2464-1

5 mL in 1 VIAL, MULTI-DOSE (22840-2464-1)
Marketing Start Date1981-09-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 22840-2464-1 [22840246401]

Velvet Mesquite Pollen SOLUTION
Marketing CategoryBLA
Application NumberBLA101833
Product TypeNON-STANDARDIZED ALLERGENIC
Marketing Start Date1981-09-15

Drug Details

Active Ingredients

IngredientStrength
PROSOPIS VELUTINA SEED.001 g/mL

NDC Crossover Matching brand name "Velvet Mesquite Pollen" or generic name "Prosopis Velutina"

NDCBrand NameGeneric Name
22840-2464Velvet Mesquite PollenProsopis velutina
22840-4457Velvet Mesquite PollenProsopis velutina
22840-5443Velvet Mesquite PollenProsopis velutina

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