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"49288-0460-3" National Drug Code (NDC)

Sorrel Mixture 10 mL in 1 VIAL, MULTI-DOSE (49288-0460-3)
(Antigen Laboratories, Inc.)

NDC Code	49288-0460-3
Package Description	10 mL in 1 VIAL, MULTI-DOSE (49288-0460-3)
Product NDC	49288-0460
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sorrel Mixture
Non-Proprietary Name	Sorrel Mixture
Dosage Form	INJECTION, SOLUTION
Usage	INTRADERMAL; SUBCUTANEOUS
Start Marketing Date	19740323
Marketing Category Name	BLA
Application Number	BLA102223
Manufacturer	Antigen Laboratories, Inc.
Substance Name	RUMEX OBTUSIFOLIUS POLLEN; RUMEX ACETOSELLA POLLEN; RUMEX ALTISSIMUS POLLEN; RUMEX SALICIFOLIUS VAR. MEXICANUS POLLEN; RUMEX CRISPUS POLLEN
Strength	.004; .004; .004; .004; .004
Strength Unit	g/mL; g/mL; g/mL; g/mL; g/mL
Pharmacy Classes	Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Increased Histamine Release [PE],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS]

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