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Vitavera

NDC 85477-513 · Oncora Pharma, LLC

Generic nameVitavera
Dosage formTABLET, CHEWABLE
RouteORAL
Active ingredient(s)VITAMIN A, ASCORBIC ACID, SODIUM ASCORBATE, VITAMIN D, ALPHA-TOCOPHEROL ACETATE, THIAMINE, RIBOFLAVIN, NIACIN, PYRIDOXINE, LEVOMEFOLIC ACID, METHYLCOBALAMIN
Strength15; 30; 1000; 4; 13; 1; 1; 30; 1; 2500; 400 [iU]/1; mg/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1
Pharmacologic classAnalogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Ascorbic Acid [CS], Folate Analog [EPC], Folic Acid [CS], Nicotinic Acid [EPC], Nicotinic Acids [CS], Vitamin A [CS], Vitamin A [EPC], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Vitamin C [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC]
Marketing categoryUNAPPROVED DRUG OTHER

Packages

85477-513-30 — 30 TABLET, CHEWABLE in 1 BOTTLE (85477-513-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

84763-007 — Dimethicone, Ascorbic Acid, Tocopherol, Panthenol, Allantoin, 84896-001 — Vitamin E, 85164-001 — KOJIC ACIDSKIN LIGHTENING, 85212-0006 — BUTYLENE GLYCOL,BUTYROSPERMUM PARKII (SHEA BUTTER),KYOUNIN YU,TOCOPHEROL,ASCORBIC ACID,NIACINAMIDE, 85212-0007 — ASCORBIC ACID,GLUTATHIONE,NIACINAMIDE,KOJIC ACID, 85212-0011 — CAFFEINE,ASCORBIC ACID,TOCOPHEROL,RETINOL,HYDROLYZED COLLAGEN,Vitamin A, 85212-0030 — ASCORBIC ACID, KOJIC ACID, 85212-0040 — DARK SPOT, 85477-322 — ASCORBIC ACID, CHOLECALCIFEROL, THIAMINE, PYRIDOXAL PHOSPHATE, FOLIC ACID, METHYLCOBALAMIN, CALCIUM CARBONATE, FERROUS GLUCONATE, POTASSIUM…, 85477-511 — Multivitamin, 85477-523 — Multivitamin, 85477-606 — Vitamin C, Vitamin D3, Vitamin B1, Vitamin B6, Vitamin B12, Folic Acid, NADH, Ubiquinone, 85477-610 — Multivitamin, 85477-623 — Multivitamin, 85477-823 — Folate, Vitamin D3, 85477-901 — Multivitamin, 85477-902 — Multivitamin, 85477-903 — Multivitamin, 85477-904 — Multivitamin, 85477-921 — Folate, Vitamin D3, +268 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.