NDC 64578-0102

Metabopath

Adenosinum Cyclophosphoricum, Adenosinum Triphosphoricum Dinatrum, Alpha-ketoglutaricum Acidum, Berberis Vulgaris, Citricum Acidum, Coenzyme A, Dna, Fumaricum Acidum, Glycyrrhiza Glabra, Hepar Sulphuris Calcareum, Lappa Major, Magnesia Phosphorica, Manganum Aceticum, Nadidum, Natrum Muriaticum, Natrum Oxalaceticum, Natrum Pyruvicum, Nicotinamidum, Pulsatilla, Pyridoxinum Hydrochloricum, Rhamnus Purshiana, Riboflavinum, Rna, Silicea, Succinicum Acidum, Sulphur, Thiaminum Hydrochloricum,

Metabopath is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Energetix Corp. The primary component is Adenosine Cyclic Phosphate; .alpha.-ketoglutaric Acid; Adenosine Triphosphate Disodium; Berberis Vulgaris Root Bark; Anhydrous Citric Acid; Coenzyme A; Herring Sperm Dna; Fumaric Acid; Glycyrrhiza Glabra; Calcium Sulfide; Arctium Lappa Root; Magnesium Phosphate, Dibasic; Manganese Acetate Tetrahydrate; Nadide; Sodium Chloride; Sodium Diethyl Oxalacetate; Sodium Pyruvate; Niacinamide; Pulsatilla Vulgaris; Pyridoxine Hydrochloride; Frangula Purshiana Bark; Riboflavin; Saccharomyces Cerevisiae Rna; Silicon Dioxide; Succinic Acid; Sulfur; Thiamine Hydrochloride; Thyroid, Bovine; Trifolium Pratense Flower; Zanthoxylum Americanum Bark; Zinc Gluconate.

Product ID64578-0102_1ca77586-6562-4101-bce9-913e1c2f6c38
NDC64578-0102
Product TypeHuman Otc Drug
Proprietary NameMetabopath
Generic NameAdenosinum Cyclophosphoricum, Adenosinum Triphosphoricum Dinatrum, Alpha-ketoglutaricum Acidum, Berberis Vulgaris, Citricum Acidum, Coenzyme A, Dna, Fumaricum Acidum, Glycyrrhiza Glabra, Hepar Sulphuris Calcareum, Lappa Major, Magnesia Phosphorica, Manganum Aceticum, Nadidum, Natrum Muriaticum, Natrum Oxalaceticum, Natrum Pyruvicum, Nicotinamidum, Pulsatilla, Pyridoxinum Hydrochloricum, Rhamnus Purshiana, Riboflavinum, Rna, Silicea, Succinicum Acidum, Sulphur, Thiaminum Hydrochloricum,
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2014-08-08
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameEnergetix Corp
Substance NameADENOSINE CYCLIC PHOSPHATE; .ALPHA.-KETOGLUTARIC ACID; ADENOSINE TRIPHOSPHATE DISODIUM; BERBERIS VULGARIS ROOT BARK; ANHYDROUS CITRIC ACID; COENZYME A; HERRING SPERM DNA; FUMARIC ACID; GLYCYRRHIZA GLABRA; CALCIUM SULFIDE; ARCTIUM LAPPA ROOT; MAGNESIUM PHOSPHATE, DIBASIC; MANGANESE ACETATE TETRAHYDRATE; NADIDE; SODIUM CHLORIDE; SODIUM DIETHYL OXALACETATE; SODIUM PYRUVATE; NIACINAMIDE; PULSATILLA VULGARIS; PYRIDOXINE HYDROCHLORIDE; FRANGULA PURSHIANA BARK; RIBOFLAVIN; SACCHAROMYCES CEREVISIAE RNA; SILICON DIOXIDE; SUCCINIC ACID; SULFUR; THIAMINE HYDROCHLORIDE; THYROID, BOVINE; TRIFOLIUM PRATENSE FLOWER; ZANTHOXYLUM AMERICANUM BARK; ZINC GLUCONATE
Active Ingredient Strength8 [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_X]/mL; [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_X]/mL; [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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 64578-0102-1

59.1 mL in 1 BOTTLE, DROPPER (64578-0102-1)
Marketing Start Date2016-05-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 64578-0102-1 [64578010201]

Metabopath LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-05-09

Drug Details


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