SEARCH RESULTS for: INACTIVE_INGREDIENT:(anhydrous dextrose) (409 results)

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NIVA THYROID (THYROID, PORCINE) TABLET

NDC Code(s): 75834-310-01, 75834-311-01, 75834-312-01, 75834-313-01, view more
75834-314-01, 75834-315-01, 75834-316-01, 75834-317-01
• Packager: NIVAGEN PHARMACEUTICALS, INC.

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LABETALOL HCL IN SODIUM CHLORIDE (LABETALOL HYDROCHLORIDE) INJECTION LABETALOL HCL IN DEXTROSE (LABETALOL HYDROCHLORIDE) INJECTION

NDC Code(s): 0143-9363-01, 0143-9363-10, 0143-9364-01, 0143-9364-10, view more
0143-9365-01, 0143-9365-10, 0143-9366-01, 0143-9366-10
• Packager: HIKMA PHARMACEUTICALS USA INC.

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OXYBUTYNIN CHLORIDE EXTENDED RELEASE (OXYBUTYNIN CHLORIDE) TABLET, EXTENDED RELEASE

NDC Code(s): 50268-627-11, 50268-627-15, 50268-628-11, 50268-628-15, view more
50268-629-11, 50268-629-13
• Packager: AVPAK
• This is a repackaged label.
• Source NDC Code(s): 62175-270, 62175-271, 62175-272

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OXYBUTYNIN CHLORIDE EXTENDED RELEASE (OXYBUTYNIN CHLORIDE) TABLET, EXTENDED RELEASE

NDC Code(s): 43353-282-30, 43353-282-53, 43353-282-60, 43353-282-80, view more
43353-284-30, 43353-284-60, 43353-322-16
• Packager: APHENA PHARMA SOLUTIONS - TENNESSEE, LLC
• This is a repackaged label.
• Source NDC Code(s): 42291-633, 42291-634, 42291-635

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OXYBUTYNIN CHLORIDE EXTENDED RELEASE (OXYBUTYNIN CHLORIDE) TABLET, EXTENDED RELEASE

NDC Code(s): 42291-633-01, 42291-633-50, 42291-634-01, 42291-634-50, view more
42291-635-01
• Packager: AVKARE
• This is a repackaged label.
• Source NDC Code(s): 62175-270, 62175-271, 62175-272

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MILRINONE LACTATE INJECTION, SOLUTION

NDC Code(s): 72485-501-01, 72485-501-10, 72485-502-01, 72485-502-10, view more
72485-503-01
• Packager: ARMAS PHARMACEUTICALS INC.

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MILRINONE LACTATE INJECTION, SOLUTION

NDC Code(s): 0143-9708-01, 0143-9708-10, 0143-9709-10, 0143-9710-10, view more
0143-9710-25
• Packager: HIKMA PHARMACEUTICALS USA INC.

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NEXTERONE (AMIODARONE HCI) INJECTION, SOLUTION

NDC Code(s): 51662-1480-1, 51662-1481-1
• Packager: HF ACQUISITION CO LLC, DBA HEALTHFIRST
• This is a repackaged label.
• Source NDC Code(s): 43066-150, 43066-360

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OXYBUTYNIN CHLORIDE EXTENDED RELEASE (OXYBUTYNIN CHLORIDE) TABLET, EXTENDED RELEASE

NDC Code(s): 68084-480-01, 68084-480-11, 68084-480-65, 68084-610-11, view more
68084-610-21
• Packager: AMERICAN HEALTH PACKAGING
• This is a repackaged label.
• Source NDC Code(s): 62175-270, 62175-271

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MILRINONE LACTATE INJECTION

NDC Code(s): 0641-6065-01, 0641-6065-10, 0641-6067-01, 0641-6067-10
• Packager: WEST-WARD PHARMACEUTICAL CORP.

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MILRINONE LACTATE IN DEXTROSE INJECTION, SOLUTION

NDC Code(s): 0143-9718-01, 0143-9718-10, 0143-9719-01, 0143-9719-10
• Packager: HIKMA PHARMACEUTICALS USA INC.

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LABETALOL HYDROCHLORIDE INJECTION

NDC Code(s): 72266-102-01, 72266-103-01
• Packager: FOSUN PHARMA USA INC.

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MILRINONE LACTATE INJECTION, SOLUTION

NDC Code(s): 83301-0016-1, 83301-0016-2, 83301-0017-1, 83301-0017-2
• Packager: MULLAN PHARMACEUTICAL INC.

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LABETALOL HYDROCHLORIDE INJECTION

NDC Code(s): 72611-734-01, 72611-738-01
• Packager: ALMAJECT, INC.

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NEXIUM (ESOMEPRAZOLE MAGNESIUM) CAPSULE, DELAYED RELEASE

NDC Code(s): 61919-509-30, 61919-509-60
• Packager: DIRECT RX
• This is a repackaged label.
• Source NDC Code(s): 0186-5040

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OXYBUTYNIN CHLORIDE EXTENDED RELEASE (OXYBUTYNIN CHLORIDE) TABLET, EXTENDED RELEASE

NDC Code(s): 50090-4192-0
• Packager: A-S MEDICATION SOLUTIONS
• This is a repackaged label.
• Source NDC Code(s): 62175-270

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PREVENTION DAILY MATTE MOISTURIZER SPF 30 (ZINC OXIDE AND HOMOSALATE) CREAM

NDC Code(s): 62742-4223-1, 62742-4223-2, 62742-4223-3
• Packager: ALLURE LABS

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FERMITIF HAND RENEWAL CREAM BROAD SPECTRUM SPF 15 SUNSCREEN (AVOBENZONE, OCTINOXATE, OCTISALATE) CREAM

NDC Code(s): 82691-148-01
• Packager: RV SKINCARE LLC

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NIOXIN SCALP RECOVERY ANTI-DANDRUFF SYSTEM (PYRITHIONE ZINC) KIT

NDC Code(s): 82157-003-20, 82157-004-20, 82157-005-10, 82157-006-99
• Packager: WELLA OPERATIONS US LLC

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PREVENTION PLUS DAILY TINTED MOISTURIZER SPF 30 (ZINC OXIDE) CREAM

NDC Code(s): 62742-4170-1, 62742-4170-2, 62742-4170-3, 62742-4170-4
• Packager: ALLURE LABS INC