SEARCH RESULTS for: oxycodone hydrochloride and ibuprofen (36 results)

SEGLENTIS (CELECOXIB AND TRAMADOL HYDROCHLORIDE) TABLET

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NDC Code(s): 66869-564-30, 66869-564-35, 66869-564-90
• Packager: KOWA PHARMACEUTICALS AMERICA, INC.

VICOPROFEN (HYDROCODONE BITARTRATE AND IBUPROFEN) TABLET, COATED

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NDC Code(s): 54868-4035-0, 54868-4035-1, 54868-4035-2, 54868-4035-3, view more
54868-4035-4
• Packager: PHYSICIANS TOTAL CARE, INC.
• This is a repackaged label.
• Source NDC Code(s): 0074-2277

DERAMSILKRX ANODYNEXA PAK (DICLOFENAC SODIUM DELAYED RELEASE TABLETS, RANITIDINE TABLETS, CAPSAICIN CREAM) KIT ...

DERAMSILKRX ANODYNEXA PAK (DICLOFENAC SODIUM DELAYED RELEASE TABLETS, RANITIDINE TABLETS, CAPSAICIN CREAM) KIT

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NDC Code(s): 0228-2551-06, 53746-253-60, 69329-310-00, 69329-323-01
• Packager: PATCHWERX LABS, INC.

HYDROCODONE BITARTRATE AND IBUPROFEN TABLET, FILM COATED

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NDC Code(s): 42549-656-30, 42549-656-60, 42549-656-90
• Packager: STAT RX USA LLC
• This is a repackaged label.
• Source NDC Code(s): 0603-3897

SULINDAC TABLET

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NDC Code(s): 33261-100-60
• Packager: AIDAREX PHARMACEUTICALS LLC
• This is a repackaged label.
• Source NDC Code(s): 42806-011

SULINDAC TABLET

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NDC Code(s): 54868-0879-0, 54868-0879-3, 54868-1118-0, 54868-1118-2, view more
54868-1118-4
• Packager: PHYSICIANS TOTAL CARE, INC.
• This is a repackaged label.
• Source NDC Code(s): 0591-5660, 0591-5661

SULINDAC TABLET

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NDC Code(s): 16590-211-30, 16590-211-60
• Packager: STAT RX USA LLC
• This is a repackaged label.
• Source NDC Code(s): 42806-011

KETOROLAC TROMETHAMINE INJECTION

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NDC Code(s): 54868-4419-0, 54868-4419-1
• Packager: PHYSICIANS TOTAL CARE, INC.
• This is a repackaged label.
• Source NDC Code(s): 64679-758

SULINDAC TABLET

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NDC Code(s): 53808-0814-1
• Packager: STATE OF FLORIDA DOH CENTRAL PHARMACY
• This is a repackaged label.
• Source NDC Code(s): 42806-011

KETOROLAC TROMETHAMINE INJECTION

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NDC Code(s): 55648-757-01, 55648-757-02, 55648-757-03, 55648-758-01, view more
55648-758-02, 55648-758-03, 55648-758-04, 55648-758-05, 55648-758-06
• Packager: WOCKHARDT LIMITED

SULINDAC TABLET

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NDC Code(s): 52959-195-14, 52959-195-15, 52959-195-18, 52959-195-20, view more
52959-195-28, 52959-195-30, 52959-195-60
• Packager: H.J. HARKINS COMPANY, INC.
• This is a repackaged label.
• Source NDC Code(s): 0591-5660

HYDROCODONE BITARTRATE AND IBUPROFEN TABLET, FILM COATED

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NDC Code(s): 54868-4976-0, 54868-4976-1, 54868-4976-2, 54868-4976-3, view more
54868-4976-4, 54868-4976-5, 54868-4976-6, 54868-4976-7
• Packager: PHYSICIANS TOTAL CARE, INC.
• This is a repackaged label.
• Source NDC Code(s): 62037-524

SPRIX (KETOROLAC TROMETHAMINE) SPRAY, METERED

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NDC Code(s): 54868-6284-0
• Packager: PHYSICIANS TOTAL CARE, INC.
• This is a repackaged label.
• Source NDC Code(s): 0517-8880

HYDROCODONE BITARTRATE AND IBUPROFEN TABLET, FILM COATED

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NDC Code(s): 33261-378-00, 33261-378-02, 33261-378-10, 33261-378-30, view more
33261-378-60, 33261-378-90
• Packager: AIDAREX PHARMACEUTICALS LLC
• This is a repackaged label.
• Source NDC Code(s): 62037-524

HYDROCODONE BITARTRATE AND IBUPROFEN TABLET, FILM COATED

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NDC Code(s): 16590-296-12, 16590-296-15, 16590-296-20, 16590-296-30, view more
16590-296-40, 16590-296-60, 16590-296-62, 16590-296-90
• Packager: STAT RX USA LLC
• This is a repackaged label.
• Source NDC Code(s): 0603-3897

SULINDAC TABLET

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NDC Code(s): 53808-0799-1
• Packager: STATE OF FLORIDA DOH CENTRAL PHARMACY
• This is a repackaged label.
• Source NDC Code(s): 23155-005

SULINDAC TABLET

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NDC Code(s): 53808-0303-1
• Packager: STATE OF FLORIDA DOH CENTRAL PHARMACY
• This is a repackaged label.
• Source NDC Code(s): 23155-006

SPRIX (KETOROLAC TROMETHAMINE) SPRAY, METERED

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NDC Code(s): 76519-1017-1
• Packager: H.J. HARKINS COMPANY, INC.
• This is a repackaged label.
• Source NDC Code(s): 0517-8880

HYDROCODONE BITARTRATE AND IBUPROFEN TABLET, FILM COATED

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NDC Code(s): 67296-1282-5
• Packager: REDPHARM DRUG, INC.
• This is a repackaged label.
• Source NDC Code(s): 62037-524

HYDROCODONE BITARTRATE TABLET, COATED

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NDC Code(s): 61919-296-30
• Packager: DIRECT RX
• This is a repackaged label.
• Source NDC Code(s): 0603-3897