NDC 49288-0655

Coca-Glycerine Control

Coca-glycerine Control

Coca-Glycerine Control is a Intradermal Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Glycerin.

Product ID49288-0655_fb54abb5-85cd-485f-9542-a2742a31bf72
NDC49288-0655
Product TypeHuman Prescription Drug
Proprietary NameCoca-Glycerine Control
Generic NameCoca-glycerine Control
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL
Marketing Start Date1974-03-23
Marketing CategoryBLA / BLA
Application NumberBLA102223
Labeler NameAntigen Laboratories, Inc.
Substance NameGLYCERIN
Active Ingredient Strength1 mL/mL
Pharm ClassesNon-Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Glycerol [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 49288-0655-1

2 mL in 1 VIAL, MULTI-DOSE (49288-0655-1)
Marketing Start Date1974-03-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49288-0655-4 [49288065504]

Coca-Glycerine Control INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0655-2 [49288065502]

Coca-Glycerine Control INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0655-3 [49288065503]

Coca-Glycerine Control INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0655-1 [49288065501]

Coca-Glycerine Control INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0655-5 [49288065505]

Coca-Glycerine Control INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
GLYCERIN.525 mL/mL

OpenFDA Data

SPL SET ID:9c75abf7-b941-4615-b059-bcc41c64d612
Manufacturer
UNII

Pharmacological Class

  • Non-Standardized Chemical Allergen [EPC]
  • Increased Histamine Release [PE]
  • Cell-mediated Immunity [PE]
  • Increased IgG Production [PE]
  • Allergens [CS]
  • Glycerol [CS]

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