NDC 0268-0642

ORRIS

Iris X Germanica Root

ORRIS is a Subcutaneous 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 ID: 0268-0642_152accc2-8563-4b11-9c7c-f61b002b30f8
• NDC: 0268-0642
• Product Type: Non-standardized Allergenic
• Proprietary Name: ORRIS
• Generic Name: Iris X Germanica Root
• Dosage Form: Injection, Solution
• Route of Administration: SUBCUTANEOUS
• Marketing Start Date: 1965-01-01
• Marketing Category: BLA / BLA
• Application Number: BLA103753
• Labeler Name: ALK-Abello, Inc.
• Substance Name: IRIS X GERMANICA ROOT
• Active Ingredient Strength: 0 g/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 0268-0642-10

10 mL in 1 VIAL, MULTI-DOSE (0268-0642-10)

• Marketing Start Date: 1965-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0268-0642-10 [00268064210]

ORRIS INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA103753
• Product Type: NON-STANDARDIZED ALLERGENIC
• Marketing Start Date: 1965-01-01

NDC 0268-0642-50 [00268064250]

ORRIS INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA103753
• Product Type: NON-STANDARDIZED ALLERGENIC
• Marketing Start Date: 1965-01-01

Drug Details

Active Ingredients

Ingredient	Strength
IRIS X GERMANICA ROOT	.05 g/mL

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

NDC	Brand Name	Generic Name
0268-0642	ORRIS	IRIS X GERMANICA ROOT
0268-6317	ORRIS	IRIS X GERMANICA ROOT