SEARCH RESULTS for: ultracet (152 results)

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ULTRACET (TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN) TABLET

NDC Code(s): 21695-143-72
• Packager: REBEL DISTRIBUTORS CORP
• This is a repackaged label.
• Source NDC Code(s): 0045-0650

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ULTRACET (TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN) TABLET, COATED

NDC Code(s): 54868-4703-1, 54868-4703-4
• Packager: PHYSICIANS TOTAL CARE, INC.
• This is a repackaged label.
• Source NDC Code(s): 50458-650

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 0615-8182-05, 0615-8182-39
• Packager: NCS HEALTHCARE OF KY, LLC DBA VANGARD LABS
• This is a repackaged label.
• Source NDC Code(s): 10702-006

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET

NDC Code(s): 53808-1039-1
• Packager: STATE OF FLORIDA DOH CENTRAL PHARMACY
• This is a repackaged label.
• Source NDC Code(s): 59746-177

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET

NDC Code(s): 67046-119-30, 67046-119-60
• Packager: CONTRACT PHARMACY SERVICES-PA
• This is a repackaged label.
• Source NDC Code(s): 59746-177

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET

NDC Code(s): 68387-500-10, 68387-500-15, 68387-500-30, 68387-500-45, view more
68387-500-60, 68387-500-90, 68387-502-90
• Packager: KELTMAN PHARMACEUTICALS INC.
• This is a repackaged label.
• Source NDC Code(s): 0591-3256, 0591-5658

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AMRIX (CYCLOBENZAPRINE HYDROCHLORIDE) CAPSULE, EXTENDED RELEASE

NDC Code(s): 21695-723-14, 21695-723-28, 21695-723-60
• Packager: REBEL DISTRIBUTORS CORP.
• This is a repackaged label.
• Source NDC Code(s): 63459-0700

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 67296-0106-1, 67296-0106-3
• Packager: REDPHARM DRUG INC.
• This is a repackaged label.
• Source NDC Code(s): 50111-563

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FEXMID (CYCLOBENZAPRINE HYDROCHLORIDE) TABLET, FILM COATED

NDC Code(s): 21695-830-30, 21695-830-60, 21695-830-72, 21695-830-90
• Packager: REBEL DISTRIBUTORS CORP
• This is a repackaged label.
• Source NDC Code(s): 68453-950

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AMRIX (CYCLOBENZAPRINE HYDROCHLORIDE) CAPSULE, EXTENDED RELEASE

NDC Code(s): 21695-953-60
• Packager: REBEL DISTRIBUTORS CORP
• This is a repackaged label.
• Source NDC Code(s): 63459-701

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FEXMID (CYCLOBENZAPRINE HYDROCHLORIDE) TABLET, FILM COATED

NDC Code(s): 16590-699-28, 16590-699-60, 16590-699-90
• Packager: STAT RX USA LLC
• This is a repackaged label.
• Source NDC Code(s): 68453-950

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 42549-508-30, 42549-508-60, 42549-508-90, 42549-641-30, view more
42549-641-60, 42549-641-90
• Packager: STAT RX USA LLC
• This is a repackaged label.
• Source NDC Code(s): 0591-3256, 0591-5658

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 66116-527-30
• Packager: MEDVANTX, INC.
• This is a repackaged label.
• Source NDC Code(s): 50111-563

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 53808-0862-1
• Packager: STATE OF FLORIDA DOH CENTRAL PHARMACY
• This is a repackaged label.
• Source NDC Code(s): 53489-591

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 53808-0639-1, 53808-0881-2
• Packager: STATE OF FLORIDA DOH CENTRAL PHARMACY
• This is a repackaged label.
• Source NDC Code(s): 65862-190, 65862-191

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AMRIX (CYCLOBENZAPRINE HYDROCHLORIDE) CAPSULE, EXTENDED RELEASE

NDC Code(s): 54868-6022-0
• Packager: PHYSICIANS TOTAL CARE, INC.
• This is a repackaged label.
• Source NDC Code(s): 63459-700

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 10544-072-00, 10544-072-02, 10544-072-09, 10544-072-10, view more
10544-072-14, 10544-072-15, 10544-072-20, 10544-072-21, 10544-072-30, 10544-072-45, 10544-072-60, 10544-072-84, 10544-072-90
• Packager: BLENHEIM PHARMACAL, INC.
• This is a repackaged label.
• Source NDC Code(s): 0591-5658

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 0440-1350-09
• Packager: LIBERTY PHARMACEUTICALS, INC.
• This is a repackaged label.
• Source NDC Code(s): 0591-5658

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 66336-581-15, 66336-581-30, 66336-581-60, 66336-581-90
• Packager: DISPENSING SOLUTIONS, INC.
• This is a repackaged label.
• Source NDC Code(s): 0591-5658

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CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 53149-4841-9
• Packager: ALL PHARMA, LLC
• This is a repackaged label.
• Source NDC Code(s): 69420-1001