"72835-550-01" National Drug Code (NDC)

NDC Code	72835-550-01
Package Description	30 CAPSULE in 1 BOTTLE (72835-550-01)
Product NDC	72835-550
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Cobalefol
Non-Proprietary Name	Vitamin
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20250516
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	V2 Pharma LLC
Substance Name	.ALPHA.-TOCOPHEROL SUCCINATE, D-; ASCORBIC ACID; CHOLECALCIFEROL; FOLIC ACID; METHYLCOBALAMIN; NIACINAMIDE; PYRIDOXINE HCL; RIBOFLAVIN 5'-PHOSPHATE; THIAMINE MONONITRATE
Strength	10.5; 90; 20; 1700; 10; 16.3; 2.5; 1.6; 1.4
Strength Unit	mg/1; mg/1; ug/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1
Pharmacy Classes	Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Photoabsorption [MoA], Photoenhancer [EPC], Photosensitizing Activity [PE], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC]