SEARCH RESULTS for: 1359105 [RxCUI] (22 results)

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ARTHROTEC (diclofenac sodium and misoprostol) tablet, film coated

NDC Code(s): 0025-1411-60, 0025-1411-90, 0025-1421-60
• Packager: Pfizer Laboratories Div Pfizer Inc

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ARTHROTEC (diclofenac sodium and misoprostol) tablet, film coated

NDC Code(s): 54868-4164-0, 54868-4164-1, 54868-4165-0, 54868-4165-1
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0025-1411, 0025-1421

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ARTHROTEC (diclofenac sodium and misoprostol) tablet, film coated

NDC Code(s): 21695-425-60
• Packager: Rebel Distributors Corp.
• This is a repackaged label.
• Source NDC Code(s): 0025-1421

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ARTHROTEC (diclofenac sodium and misoprostol) tablet, film coated

NDC Code(s): 16590-024-30, 16590-024-60
• Packager: STAT Rx USA LLC
• This is a repackaged label.
• Source NDC Code(s): 0025-1421

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DICLOENAC SODIUM AND MISOPROSTOL DR (dicloenac sodium and misoprostol) tablet

NDC Code(s): 80425-0273-1
• Packager: Advanced Rx Pharmacy of Tennessee, LLC
• This is a repackaged label.
• Source NDC Code(s): 42571-134

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DICLOFENAC SODIUM AND MISOPROSTOL DELAYED-RELEASE (diclofenac sodium and misoprostol) tablet, delayed release

NDC Code(s): 10544-955-14
• Packager: Blenheim Pharmacal, Inc.
• This is a repackaged label.
• Source NDC Code(s): 42367-111

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DICLOFENAC SODIUM AND MISOPROSTOL DELAYED-RELEASE (diclofenac sodium and misoprostol) tablet, delayed release

NDC Code(s): 42367-110-06, 42367-110-09, 42367-111-06
• Packager: Eagle Pharmaceuticals, Inc.

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DICLOFENAC SODIUM AND MISOPROSTOL DR (diclofenac sodium and misoprostol) tablet, film coated

NDC Code(s): 80425-0272-1
• Packager: Advanced Rx Pharmacy of Tennessee, LLC
• This is a repackaged label.
• Source NDC Code(s): 59762-0029

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DICLOFENAC SODIUM AND MISOPROSTOL tablet, delayed release

NDC Code(s): 0591-0397-19, 0591-0397-60, 0591-0398-60
• Packager: Actavis Pharma, Inc.

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DICLOFENAC SODIUM AND MISOPROSTOL tablet, delayed release

NDC Code(s): 65162-436-03, 65162-436-06, 65162-436-09, 65162-436-10, view more
65162-438-03, 65162-438-06, 65162-438-10
• Packager: Amneal Pharmaceuticals LLC

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DICLOFENAC SODIUM AND MISOPROSTOL tablet, delayed release

NDC Code(s): 50090-4618-0
• Packager: A-S Medication Solutions
• This is a repackaged label.
• Source NDC Code(s): 65162-438

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DICLOFENAC SODIUM AND MISOPROSTOL tablet, delayed release

NDC Code(s): 42291-232-60, 42291-232-90, 42291-233-60
• Packager: AvKARE
• This is a repackaged label.
• Source NDC Code(s): 0591-0397, 0591-0398

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DICLOFENAC SODIUM AND MISOPROSTOL tablet, delayed release

NDC Code(s): 10544-949-14
• Packager: Blenheim Pharmacal, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0591-0398

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DICLOFENAC SODIUM AND MISOPROSTOL tablet, delayed release

NDC Code(s): 68001-231-06, 68001-232-06
• Packager: BluePoint Laboratories

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DICLOFENAC SODIUM AND MISOPROSTOL tablet, delayed release

NDC Code(s): 71335-1183-1, 71335-1183-2, 71335-1183-3, 71335-1183-4, view more
71335-1183-5
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 65162-438

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DICLOFENAC SODIUM AND MISOPROSTOL tablet, delayed release

NDC Code(s): 68788-7103-3, 68788-7103-6
• Packager: Preferred Pharmaceuticals Inc.
• This is a repackaged label.
• Source NDC Code(s): 65162-438

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DICLOFENAC SODIUM AND MISOPROSTOL tablet, film coated

NDC Code(s): 61919-094-60
• Packager: DIRECT RX
• This is a repackaged label.
• Source NDC Code(s): 59762-0029

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DICLOFENAC SODIUM AND MISOPROSTOL tablet, film coated

NDC Code(s): 59762-0028-1, 59762-0028-2, 59762-0029-1
• Packager: Greenstone LLC

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DICLOFENAC SODIUM MISOPROSTOL (diclofenac sodium and misoprostol) tablet, delayed release

NDC Code(s): 75834-264-60, 75834-264-90, 75834-265-60
• Packager: Nivagen Pharmaceuticals, Inc.

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DICLOFENAC SODIUM MISOPROSTOL (diclofenac sodium and misoprostol) tablet, delayed release

NDC Code(s): 71205-865-00, 71205-865-30, 71205-865-55, 71205-865-60, view more
71205-865-64, 71205-865-72, 71205-865-90, 71205-866-00, 71205-866-30, 71205-866-55, 71205-866-60, 71205-866-64, 71205-866-72, 71205-866-90
• Packager: Proficient Rx LP
• This is a repackaged label.
• Source NDC Code(s): 75834-264, 75834-265