NDC 22840-5711

Cantaloupe Muskmelon

Cucumis Melo

Cantaloupe Muskmelon 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 Muskmelon.

• Product ID: 22840-5711_79ebe8af-3396-1b14-e053-2a91aa0a89ba
• NDC: 22840-5711
• Product Type: Non-standardized Allergenic
• Proprietary Name: Cantaloupe Muskmelon
• Generic Name: Cucumis Melo
• 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: MUSKMELON
• Active Ingredient Strength: 0 g/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 22840-5711-2

10 mL in 1 VIAL, MULTI-DOSE (22840-5711-2)

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

NDC SPL Data Element Entries

NDC 22840-5711-2 [22840571102]

Cantaloupe Muskmelon SOLUTION

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

NDC 22840-5711-5 [22840571105]

Cantaloupe Muskmelon SOLUTION

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

Drug Details

Active Ingredients

Ingredient	Strength
MUSKMELON	.05 g/mL

NDC Crossover Matching brand name "Cantaloupe Muskmelon" or generic name "Cucumis Melo"

NDC	Brand Name	Generic Name
22840-5711	Cantaloupe Muskmelon	Cucumis melo
0268-6146	HONEYDEW	CUCUMIS MELO