NDC 22840-5775

Ocean Perch

Sebastes Alutus

Ocean Perch 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 Pacific Ocean Perch.

Product ID22840-5775_79ebe8af-3396-1b14-e053-2a91aa0a89ba
NDC22840-5775
Product TypeNon-standardized Allergenic
Proprietary NameOcean Perch
Generic NameSebastes Alutus
Dosage FormSolution
Route of AdministrationINTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS
Marketing Start Date1981-09-15
Marketing CategoryBLA / BLA
Application NumberBLA101833
Labeler NameGreer Laboratories, Inc.
Substance NamePACIFIC OCEAN PERCH
Active Ingredient Strength0 g/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 22840-5775-2

10 mL in 1 VIAL, MULTI-DOSE (22840-5775-2)
Marketing Start Date1981-09-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 22840-5775-5 [22840577505]

Ocean Perch SOLUTION
Marketing CategoryBLA
Application NumberBLA101833
Product TypeNON-STANDARDIZED ALLERGENIC
Marketing Start Date1981-09-15

NDC 22840-5775-2 [22840577502]

Ocean Perch SOLUTION
Marketing CategoryBLA
Application NumberBLA101833
Product TypeNON-STANDARDIZED ALLERGENIC
Marketing Start Date1981-09-15

Drug Details

Active Ingredients

IngredientStrength
PACIFIC OCEAN PERCH.05 g/mL

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