NDC 0268-6317

ORRIS

Iris X Germanica Root

ORRIS is a Percutaneous Injection, Solution in the Non-standardized Allergenic category. It is labeled and distributed by Alk-abello, Inc.. The primary component is Iris X Germanica Root.

Product ID0268-6317_06c812ac-2bfd-444c-b2b9-50076167486c
NDC0268-6317
Product TypeNon-standardized Allergenic
Proprietary NameORRIS
Generic NameIris X Germanica Root
Dosage FormInjection, Solution
Route of AdministrationPERCUTANEOUS
Marketing Start Date1965-01-01
Marketing CategoryBLA / BLA
Application NumberBLA103753
Labeler NameALK-Abello, Inc.
Substance NameIRIS X GERMANICA ROOT
Active Ingredient Strength0 g/mL
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0268-6317-06

5 mL in 1 VIAL, MULTI-DOSE (0268-6317-06)
Marketing Start Date1965-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0268-6317-06 [00268631706]

ORRIS INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA103753
Product TypeNON-STANDARDIZED ALLERGENIC
Marketing Start Date1965-01-01

Drug Details

Active Ingredients

IngredientStrength
IRIS X GERMANICA ROOT.05 g/mL

NDC Crossover Matching brand name "ORRIS" or generic name "Iris X Germanica Root"

NDCBrand NameGeneric Name
0268-0642ORRISIRIS X GERMANICA ROOT
0268-6317ORRISIRIS X GERMANICA ROOT

Trademark Results [ORRIS]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ORRIS
ORRIS
97389914 not registered Live/Pending
Westwood Footwear Corporation
2022-04-29

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