NDC 22840-2618

Phoma betae

Phoma Betae

Phoma betae 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 Pleospora Betae.

• Product ID: 22840-2618_77436178-2957-6a77-e053-2a91aa0a873e
• NDC: 22840-2618
• Product Type: Non-standardized Allergenic
• Proprietary Name: Phoma betae
• Generic Name: Phoma Betae
• Dosage Form: Solution
• Route of Administration: INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS
• Marketing Start Date: 1981-09-15
• Marketing Category: BLA / BLA
• Application Number: BLA101833
• Labeler Name: Greer Laboratories, Inc.
• Substance Name: PLEOSPORA BETAE
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 22840-2618-1

5 mL in 1 VIAL, MULTI-DOSE (22840-2618-1)

• Marketing Start Date: 1981-09-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 22840-2618-1 [22840261801]

Phoma betae SOLUTION

• Marketing Category: BLA
• Application Number: BLA101833
• Product Type: NON-STANDARDIZED ALLERGENIC
• Marketing Start Date: 1981-09-15

Drug Details

Active Ingredients

Ingredient	Strength
PLEOSPORA BETAE	.001 g/mL

Pharmacological Class

• Increased Histamine Release [PE]
• Cell-mediated Immunity [PE]
• Increased IgG Production [PE]
• Fungal Proteins [CS]
• Allergens [CS]
• Non-Standardized Fungal Allergenic Extract [EPC]

NDC Crossover Matching brand name "Phoma betae" or generic name "Phoma Betae"

NDC	Brand Name	Generic Name
22840-2618	Phoma betae	Phoma betae
22840-2674	Phoma betae	Phoma betae
22840-5632	Phoma betae	Phoma betae
49643-116	Phoma	Phoma betae