NDC 22840-5443

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 ID22840-5443_83d281e9-375b-7e6c-e053-2991aa0a6f0e
NDC22840-5443
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 22840-5443-2

10 mL in 1 VIAL, MULTI-DOSE (22840-5443-2)
Marketing Start Date1981-09-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 22840-5443-5 [22840544305]

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

NDC 22840-5443-4 [22840544304]

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

NDC 22840-5443-2 [22840544302]

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.05 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

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.