Last Updated: August 3, 2026

MULTIPLE VITAMINS INJECTION ADULT Drug Patent Profile

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Which patents cover Multiple Vitamins Injection Adult, and when can generic versions of Multiple Vitamins Injection Adult launch?

Multiple Vitamins Injection Adult is a drug marketed by Apotex and is included in two NDAs.

The generic ingredient in MULTIPLE VITAMINS INJECTION ADULT is alpha-tocopherol acetate; ascorbic acid; biotin; cholecalciferol; cyanocobalamin; dexpanthenol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin 5'-phosphate sodium; thiamine hydrochloride; vitamin a palmitate; vitamin k. There are two drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the alpha-tocopherol acetate; ascorbic acid; biotin; cholecalciferol; cyanocobalamin; dexpanthenol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin 5'-phosphate sodium; thiamine hydrochloride; vitamin a palmitate; vitamin k profile page.

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Summary for MULTIPLE VITAMINS INJECTION ADULT

US Patents:	0
Applicants:	1
NDAs:	2

US Patents and Regulatory Information for MULTIPLE VITAMINS INJECTION ADULT

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Glossary

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	TE	Type	RLD	RS	Patent No.	Patent Expiration	Product	Substance	Delist Req.	Exclusivity Expiration
Apotex	MULTIPLE VITAMINS INJECTION ADULT	alpha-tocopherol acetate; ascorbic acid; biotin; cholecalciferol; cyanocobalamin; dexpanthenol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin 5'-phosphate sodium; thiamine hydrochloride; vitamin a palmitate; vitamin k	SOLUTION;INTRAVENOUS	210273-001	Apr 9, 2026	AP	RX	No	No	⤷ Start Trial	⤷ Start Trial				⤷ Start Trial
Apotex	MULTIPLE VITAMINS INJECTION ADULT	alpha-tocopherol acetate; ascorbic acid; biotin; cholecalciferol; cyanocobalamin; dexpanthenol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin 5'-phosphate sodium; thiamine hydrochloride; vitamin a palmitate; vitamin k	SOLUTION;INTRAVENOUS	210672-001	Apr 9, 2026	AP	RX	No	No	⤷ Start Trial	⤷ Start Trial				⤷ Start Trial
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>TE	>Type	>RLD	>RS	>Patent No.	>Patent Expiration	>Product	>Substance	>Delist Req.	>Exclusivity Expiration

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