Product NDC: | 36987-2212 |
Proprietary Name: | Cotton Seed |
Non Proprietary Name: | Cotton Seed |
Active Ingredient(s): | .1 g/mL & nbsp; Cotton Seed |
Administration Route(s): | INTRADERMAL; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 36987-2212 |
Labeler Name: | Nelco Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA102192 |
Marketing Category: | BLA |
Start Marketing Date: | 19720829 |
Package NDC: | 36987-2212-3 |
Package Description: | 30 mL in 1 VIAL, MULTI-DOSE (36987-2212-3) |
NDC Code | 36987-2212-3 |
Proprietary Name | Cotton Seed |
Package Description | 30 mL in 1 VIAL, MULTI-DOSE (36987-2212-3) |
Product NDC | 36987-2212 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Cotton Seed |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRADERMAL; SUBCUTANEOUS |
Start Marketing Date | 19720829 |
Marketing Category Name | BLA |
Labeler Name | Nelco Laboratories, Inc. |
Substance Name | COTTON SEED |
Strength Number | .1 |
Strength Unit | g/mL |
Pharmaceutical Classes | Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Seed Storage Proteins [Chemical/Ingredient] |