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Generated: February 19, 2018

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Codeine phosphate; pseudoephedrine hydrochloride; triprolidine hydrochloride - Generic Drug Details

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What are the generic sources for codeine phosphate; pseudoephedrine hydrochloride; triprolidine hydrochloride and what is the scope of codeine phosphate; pseudoephedrine hydrochloride; triprolidine hydrochloride freedom to operate?

Codeine phosphate; pseudoephedrine hydrochloride; triprolidine hydrochloride
is the generic ingredient in four branded drugs marketed by Glaxosmithkline, Sti Pharma Llc, Cenci, and Wockhardt, and is included in four NDAs. Additional information is available in the individual branded drug profile pages.

There are nineteen drug master file entries for codeine phosphate; pseudoephedrine hydrochloride; triprolidine hydrochloride. One supplier is listed for this compound.
Summary for codeine phosphate; pseudoephedrine hydrochloride; triprolidine hydrochloride
Pharmacology for codeine phosphate; pseudoephedrine hydrochloride; triprolidine hydrochloride

US Patents and Regulatory Information for codeine phosphate; pseudoephedrine hydrochloride; triprolidine hydrochloride

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Cenci TRIPROLIDINE AND PSEUDOEPHEDRINE HYDROCHLORIDES W/ CODEINE codeine phosphate; pseudoephedrine hydrochloride; triprolidine hydrochloride SYRUP;ORAL 089018-001 Jul 23, 1986 DISCN No No ➤ Sign Up ➤ Sign Up ➤ Sign Up
Glaxosmithkline ACTIFED W/ CODEINE codeine phosphate; pseudoephedrine hydrochloride; triprolidine hydrochloride SYRUP;ORAL 012575-003 Apr 4, 1984 DISCN No No ➤ Sign Up ➤ Sign Up ➤ Sign Up
Wockhardt TRIPROLIDINE HCL, PSEUDOEPHEDRINE HCL AND CODEINE PHOSPHATE codeine phosphate; pseudoephedrine hydrochloride; triprolidine hydrochloride SYRUP;ORAL 088833-001 Nov 16, 1984 DISCN No No ➤ Sign Up ➤ Sign Up ➤ Sign Up
Sti Pharma Llc TRIACIN-C codeine phosphate; pseudoephedrine hydrochloride; triprolidine hydrochloride SYRUP;ORAL 088704-001 Mar 22, 1985 RX No Yes ➤ 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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