"50181-0070-1" National Drug Code (NDC)

Neurobalance Pro 30 mL in 1 BOTTLE, SPRAY (50181-0070-1)
(The Wellness Center for Reseach and Education, Inc.)

NDC Code50181-0070-1
Package Description30 mL in 1 BOTTLE, SPRAY (50181-0070-1)
Product NDC50181-0070
Product Type NameHUMAN OTC DRUG
Proprietary NameNeurobalance Pro
Non-Proprietary NameGaba (gamma-aminobutyric Acid), L-glutamic Acid, Norepinephrine (bitartrate), Acetylcholine Chloride, L-dopa, Serotonin (hydrochloride), Thyroidinum (suis), Adrenalinum, Baryta Carbonica, Calcarea Carbonica, Anacardium Orientale, Adrenocorticotrophin, Stramonium
Dosage FormLIQUID
UsageORAL
Start Marketing Date20191119
Marketing Category NameUNAPPROVED HOMEOPATHIC
ManufacturerThe Wellness Center for Reseach and Education, Inc.
Substance Name.GAMMA.-AMINOBUTYRIC ACID; GLUTAMIC ACID; NOREPINEPHRINE BITARTRATE; ACETYLCHOLINE CHLORIDE; LEVODOPA; SEROTONIN HYDROCHLORIDE; THYROID, PORCINE; EPINEPHRINE; BARIUM CARBONATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SEMECARPUS ANACARDIUM JUICE; CORTICOTROPIN; DATURA STRAMONIUM
Strength6; 6; 6; 6; 6; 6; 6; 10; 6; 6; 8; 14; 30
Strength Unit[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL

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