BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE
NDC Code(s): 70436-010-04, 70436-010-06, 70436-010-02, 70436-011-04, 70436-011-06, 70436-011-02
Packager: Slate Run Pharmaceuticals, LLC
BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE
NDC Code(s): 58657-710-30, 58657-710-90, 58657-710-50, 58657-711-30, 58657-711-90, 58657-711-50
Packager: Method Pharmaceuticals, LLC
SODIUM FLUORIDE PASTE, DENTIFRICE
NDC Code(s): 55346-0718-2, 55346-0718-1
Packager: Dental Technologies, Inc
LIDOCAINE OINTMENT
NDC Code(s): 70518-2355-0
Packager: REMEDYREPACK INC.
This is a repackaged label.
Source NDC Code(s): 52565-008
Acetaminophen LIQUID
NDC Code(s): 55700-553-04
Packager: Lake Erie Medical DBA Quality Care Products LLC
This is a repackaged label.
Source NDC Code(s): 0904-1985
LIDOCAINE OINTMENT
NDC Code(s): 68788-7486-5
Packager: Preferred Pharmaceuticals Inc.
This is a repackaged label.
Source NDC Code(s): 70512-027
LIDOCAINE OINTMENT
NDC Code(s): 68788-6319-3, 68788-6319-5
Packager: Preferred Pharmaceuticals Inc.
This is a repackaged label.
Source NDC Code(s): 68462-418
LIDOCAINE OINTMENT
NDC Code(s): 53217-248-01
Packager: Aidarex Pharmaceuticals LLC
This is a repackaged label.
Source NDC Code(s): 52565-008
BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE
NDC Code(s): 69844-010-01, 69844-010-02, 69844-010-03, 69844-011-01, 69844-011-02, 69844-011-03
Packager: Graviti Pharmaceuticals Private Limited