SEARCH RESULTS for: trifluoperazine (12 results)

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TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 51079-572-01, 51079-572-20, 51079-573-01, 51079-573-20, view more
51079-574-01, 51079-574-20, 51079-575-01, 51079-575-20
• Packager: MYLAN INSTITUTIONAL INC.
• This is a repackaged label.
• Source NDC Code(s): 0378-2401, 0378-2402, 0378-2405, 0378-2410

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TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 0781-8028-01, 0781-8032-01, 0781-8034-01, 0781-8036-01
• Packager: SANDOZ INC.

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TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 0378-2401-01, 0378-2402-01, 0378-2405-01, 0378-2410-01
• Packager: MYLAN PHARMACEUTICALS INC.

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TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 53808-0629-1, 53808-0819-1
• Packager: STATE OF FLORIDA DOH CENTRAL PHARMACY
• This is a repackaged label.
• Source NDC Code(s): 0378-2402, 0378-2410

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TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 72162-2206-1
• Packager: BRYANT RANCH PREPACK
• This is a repackaged label.
• Source NDC Code(s): 0781-8032

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TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 72162-2207-1
• Packager: BRYANT RANCH PREPACK
• This is a repackaged label.
• Source NDC Code(s): 0781-8034

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TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 72162-2205-1
• Packager: BRYANT RANCH PREPACK
• This is a repackaged label.
• Source NDC Code(s): 0781-8036

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TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 72162-2204-1
• Packager: BRYANT RANCH PREPACK
• This is a repackaged label.
• Source NDC Code(s): 0781-8028

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TRIFLUOPERAZINE TABLET, FILM COATED

NDC Code(s): 16590-305-30, 16590-305-60, 16590-305-90
• Packager: STAT RX USA LLC
• This is a repackaged label.
• Source NDC Code(s): 0781-1032

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TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 70518-2095-0
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 0378-2402

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TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 70518-2106-0
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 0378-2405

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PRASTERA (PRASTERONE AND IBUPROFEN) KIT

NDC Code(s): 55607-400-10
• Packager: HEALTH SCIENCE FUNDING, LLC
• This is a repackaged label.
• Source NDC Code(s): 25000-121