SEARCH RESULTS for: rx act ibuprofen childrens (351 results)

RX ACT IBUPROFEN CHILDRENS (IBUPROFEN) SUSPENSION

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NDC Code(s): 37808-897-26
• Packager: H E B

PRASTERA (PRASTERONE AND IBUPROFEN) KIT

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

CARBAMAZEPINE TABLET, CHEWABLE CARBAMAZEPINE TABLET CARBAMAZEPINE TABLET, EXTENDED RELEASE CARBAMAZEPINE SUSPENSION ...

CARBAMAZEPINE TABLET, CHEWABLE CARBAMAZEPINE TABLET CARBAMAZEPINE TABLET, EXTENDED RELEASE CARBAMAZEPINE SUSPENSION

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NDC Code(s): 51672-4005-1, 51672-4005-2, 51672-4005-3, 51672-4041-0, view more
51672-4041-1, 51672-4041-2, 51672-4041-9, 51672-4047-9, 51672-4050-1, 51672-4123-1, 51672-4123-3, 51672-4123-6, 51672-4124-1, 51672-4124-3, 51672-4124-6, 51672-4125-1, 51672-4125-3, 51672-4125-6
• Packager: TARO PHARMACEUTICALS U.S.A., INC.

CARBAMAZEPINE TABLET

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NDC Code(s): 51407-215-01, 51407-215-10
• Packager: GOLDEN STATE MEDICAL SUPPLY, INC.
• This is a repackaged label.
• Source NDC Code(s): 51672-4005

CARBAMAZEPINE TABLET, CHEWABLE

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NDC Code(s): 60429-934-05
• Packager: GOLDEN STATE MEDICAL SUPPLY, INC.
• This is a repackaged label.
• Source NDC Code(s): 51672-4041

CARBAMAZEPINE TABLET, EXTENDED RELEASE

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NDC Code(s): 51407-895-01, 51407-896-01, 51407-897-01
• Packager: GOLDEN STATE MEDICAL SUPPLY, INC.
• This is a repackaged label.
• Source NDC Code(s): 51672-4123, 51672-4124, 51672-4125

CARBAMAZEPINE TABLET

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NDC Code(s): 43063-328-12, 43063-328-30
• Packager: PD-RX PHARMACEUTICALS, INC.
• This is a repackaged label.
• Source NDC Code(s): 51672-4005

VIVA CT PRENATAL (FOLIC ACID, FERROUS FUMARATE, ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, THIAMINE MONONITRATE, RIBOFLAV...

VIVA CT PRENATAL (FOLIC ACID, FERROUS FUMARATE, ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, THIAMINE MONONITRATE, RIBOFLAVIN, PYRIDOXINE HYDROCHLORIDE, CYANOCOBALAMIN, ZINC OXIDE, CUPRIC SULFATE ANHYDROUS, AND SELENOMETHIONINE) TABLET, CHEWABLE

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NDC Code(s): 64661-811-30
• Packager: JAYMAC PHARMACEUTICALS LLC

THERAPROFEN-90 (IBUPROFEN, .GAMMA.-AMINOBUTYRIC ACID) KIT

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NDC Code(s): 52959-076-60, 68405-088-36
• Packager: PHYSICIAN THERAPEUTICS LLC

THERAPROFEN-800 (IBUPROFEN, .GAMMA.-AMINOBUTYRIC ACID) KIT

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NDC Code(s): 52959-077-30, 68405-188-36
• Packager: PHYSICIAN THERAPEUTICS LLC

THERAPROFEN-60 (IBUPROFEN, .GAMMA.-AMINOBUTYRIC ACID) KIT

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NDC Code(s): 52959-076-60, 68405-880-26
• Packager: PHYSICIAN THERAPEUTICS LLC

ESCITALOPRAM TABLET, FILM COATED

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NDC Code(s): 42549-672-28, 42549-672-30, 42549-672-60, 42549-672-90
• Packager: STAT RX USA LLC
• This is a repackaged label.
• Source NDC Code(s): 0093-5852

VALSARTAN TABLET

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NDC Code(s): 63187-655-30, 63187-655-60, 63187-655-90
• Packager: PROFICIENT RX LP
• This is a repackaged label.
• Source NDC Code(s): 43547-370

SAVELLA (MILNACIPRAN HYDROCHLORIDE) TABLET, FILM COATED

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NDC Code(s): 55154-4626-8
• Packager: CARDINAL HEALTH 107, LLC
• This is a repackaged label.
• Source NDC Code(s): 0456-1550

SERTRALINE HYDROCHLORIDE TABLET

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NDC Code(s): 63187-795-30, 63187-795-60, 63187-795-90
• Packager: PROFICIENT RX LP
• This is a repackaged label.
• Source NDC Code(s): 69097-835

SERTRALINE HYDROCHLORIDE TABLET

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NDC Code(s): 63187-859-30, 63187-859-60, 63187-859-90
• Packager: PROFICIENT RX LP
• This is a repackaged label.
• Source NDC Code(s): 69097-833

VALSARTAN TABLET, FILM COATED

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NDC Code(s): 71205-301-30, 71205-301-60, 71205-301-90
• Packager: PROFICIENT RX LP
• This is a repackaged label.
• Source NDC Code(s): 33342-065

VALSARTAN TABLET

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NDC Code(s): 72789-281-60
• Packager: PD-RX PHARMACEUTICALS, INC.
• This is a repackaged label.
• Source NDC Code(s): 59746-362

SERTRALINE TABLET, FILM COATED

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NDC Code(s): 63187-055-30, 63187-055-60, 63187-055-90, 63187-212-30, view more
63187-212-60, 63187-212-90, 63187-478-30, 63187-478-60, 63187-478-90
• Packager: PROFICIENT RX LP
• This is a repackaged label.
• Source NDC Code(s): 68180-351, 68180-352, 68180-353

SERTRALINE HYDROCHLORIDE TABLET, FILM COATED

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NDC Code(s): 61919-345-30
• Packager: DIRECT RX
• This is a repackaged label.
• Source NDC Code(s): 16729-216