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Last Updated: November 4, 2024

M.V.I. ADULT Drug Patent Profile


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Which patents cover M.v.i. Adult, and when can generic versions of M.v.i. Adult launch?

M.v.i. Adult is a drug marketed by Hospira and is included in two NDAs.

The generic ingredient in M.V.I. ADULT is ascorbic acid; biotin; cyanocobalamin; dexpanthenol; ergocalciferol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin 5'-phosphate sodium; thiamine hydrochloride; vitamin a; vitamin e; vitamin k. There are six drug master file entries for this compound. Additional details are available on the ascorbic acid; biotin; cyanocobalamin; dexpanthenol; ergocalciferol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin 5'-phosphate sodium; thiamine hydrochloride; vitamin a; vitamin e; vitamin k profile page.

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Summary for M.V.I. ADULT
US Patents:0
Applicants:1
NDAs:2
Drug Prices: Drug price information for M.V.I. ADULT
What excipients (inactive ingredients) are in M.V.I. ADULT?M.V.I. ADULT excipients list
DailyMed Link:M.V.I. ADULT at DailyMed
Drug patent expirations by year for M.V.I. ADULT
Drug Prices for M.V.I. ADULT

See drug prices for M.V.I. ADULT

US Patents and Regulatory Information for M.V.I. ADULT

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Hospira M.V.I. ADULT ascorbic acid; biotin; cyanocobalamin; dexpanthenol; ergocalciferol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin 5'-phosphate sodium; thiamine hydrochloride; vitamin a; vitamin e; vitamin k INJECTABLE;INTRAVENOUS 021625-001 Jan 30, 2004 DISCN Yes No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Hospira M.V.I. ADULT (PHARMACY BULK PACKAGE) ascorbic acid; biotin; cyanocobalamin; dexpanthenol; ergocalciferol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin 5'-phosphate sodium; thiamine hydrochloride; vitamin a; vitamin e; vitamin k INJECTABLE;INTRAVENOUS 021643-001 Feb 18, 2004 DISCN Yes No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
>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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