NDC 49288-0116

Cottonseed

Cottonseed

Cottonseed is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Cotton Seed.

• Product ID: 49288-0116_afc65820-1d95-4bc6-81a6-ef5ca82cbd81
• NDC: 49288-0116
• Product Type: Human Prescription Drug
• Proprietary Name: Cottonseed
• Generic Name: Cottonseed
• Dosage Form: Injection, Solution
• Route of Administration: INTRADERMAL; SUBCUTANEOUS
• Marketing Start Date: 1974-03-23
• Marketing Category: BLA / BLA
• Application Number: BLA102223
• Labeler Name: Antigen Laboratories, Inc.
• Substance Name: COTTON SEED
• Active Ingredient Strength: 0 g/mL
• Pharm Classes: Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Plant Proteins [CS],Seed Storage Proteins [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 49288-0116-1

2 mL in 1 VIAL, MULTI-DOSE (49288-0116-1)

• Marketing Start Date: 1974-03-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 49288-0116-2 [49288011602]

Cottonseed INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

NDC 49288-0116-1 [49288011601]

Cottonseed INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

NDC 49288-0116-5 [49288011605]

Cottonseed INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

NDC 49288-0116-4 [49288011604]

Cottonseed INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

NDC 49288-0116-3 [49288011603]

Cottonseed INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102223
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1974-03-23
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
COTTON SEED	.05 g/mL

OpenFDA Data

• SPL SET ID: 040dacaf-4ccf-425a-9b40-586176b7631d
• Manufacturer:
  • Antigen Laboratories, Inc.
• UNII:
  • 3SW678MX72
  • 4110YT348C
  • DI0ZRJ0MXN
• RxNorm Concept Unique ID - RxCUI:
  • 891505
  • 978958
  • 966958

Pharmacological Class

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

NDC Crossover Matching brand name "Cottonseed" or generic name "Cottonseed"

NDC	Brand Name	Generic Name
22840-1554	Cottonseed	Gossypium hirsutum
22840-1555	Cottonseed	Gossypium hirsutum
22840-5509	Cottonseed	Gossypium hirsutum
49288-0116	Cottonseed	Cottonseed
49643-005	Cottonseed	Cottonseed
0268-0612	COTTON SEED	COTTONSEED
0268-6304	COTTON SEED	Cottonseed