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Generated: June 17, 2019

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Homatropine methylbromide; hydrocodone bitartrate - Generic Drug Details

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What are the generic drug sources for homatropine methylbromide; hydrocodone bitartrate and what is the scope of homatropine methylbromide; hydrocodone bitartrate patent protection?

Homatropine methylbromide; hydrocodone bitartrate is the generic ingredient in five branded drugs marketed by Genus Lifesciences, Abhai Llc, Actavis Mid Atlantic, Hi Tech Pharma, Ivax Sub Teva Pharms, Novel Labs Inc, Paddock Llc, Torrent, Wockhardt Bio Ag, Halsey, Actavis Elizabeth, Avanthi Inc, and King Pharms, and is included in fourteen NDAs. Additional information is available in the individual branded drug profile pages.

There are five drug master file entries for homatropine methylbromide; hydrocodone bitartrate. Thirteen suppliers are listed for this compound.

Summary for homatropine methylbromide; hydrocodone bitartrate
Pharmacology for homatropine methylbromide; hydrocodone bitartrate

US Patents and Regulatory Information for homatropine methylbromide; hydrocodone bitartrate

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Novel Labs Inc HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE homatropine methylbromide; hydrocodone bitartrate SYRUP;ORAL 203535-001 Feb 13, 2017 AA RX No No ➤ Sign Up ➤ Sign Up ➤ Sign Up
Ivax Sub Teva Pharms HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE homatropine methylbromide; hydrocodone bitartrate SYRUP;ORAL 040285-001 Jul 19, 1999 DISCN No No ➤ Sign Up ➤ Sign Up ➤ Sign Up
King Pharms TUSSIGON homatropine methylbromide; hydrocodone bitartrate TABLET;ORAL 088508-001 Jul 30, 1985 AA RX No Yes ➤ Sign Up ➤ Sign Up ➤ Sign Up
Genus Lifesciences HYCODAN homatropine methylbromide; hydrocodone bitartrate TABLET;ORAL 005213-001 Jul 26, 1988 DISCN Yes No ➤ Sign Up ➤ Sign Up ➤ Sign Up
Halsey HYDROPANE homatropine methylbromide; hydrocodone bitartrate SYRUP;ORAL 088066-001 Jun 28, 1985 DISCN No 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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