SEARCH RESULTS for: 993541 [RxCUI] (97 results)

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BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 68071-2707-3
• Packager: NuCare Pharmaceuticals,Inc.
• This is a repackaged label.
• Source NDC Code(s): 16729-443

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BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 68788-7786-1, 68788-7786-3, 68788-7786-6, 68788-7786-8, view more
68788-7786-9
• Packager: Preferred Pharmaceuticals Inc.
• This is a repackaged label.
• Source NDC Code(s): 16729-443

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BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 71205-504-30, 71205-504-60, 71205-504-90
• Packager: Proficient Rx LP
• This is a repackaged label.
• Source NDC Code(s): 16729-443

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BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 55700-849-30
• Packager: Quality Care Products, LLC
• This is a repackaged label.
• Source NDC Code(s): 16729-443

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BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 70518-2051-0
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 16729-443

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BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 70518-2458-0, 70518-2458-1, 70518-2458-2, 70518-2458-3
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 16729-443

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BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 16571-862-03, 16571-862-09, 16571-862-10, 16571-862-50, view more
16571-863-03, 16571-863-09, 16571-863-10, 16571-863-50
• Packager: Rising Pharma Holdings, Inc.

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BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 47335-954-13, 47335-954-81, 47335-954-83
• Packager: Sun Pharmaceutical Industries, Inc.

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BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 63304-723-05, 63304-723-30, 63304-723-90
• Packager: Sun Pharmaceutical Industries, Inc.

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BUPROPION HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 33261-627-30, 33261-680-30, 33261-680-60, 33261-680-90
• Packager: Aidarex Pharmaceuticals LLC
• This is a repackaged label.
• Source NDC Code(s): 10370-101, 10370-102

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BUPROPION HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 60687-312-01, 60687-312-11
• Packager: American Health Packaging
• This is a repackaged label.
• Source NDC Code(s): 10370-101

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BUPROPION HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 0115-6811-02, 0115-6811-08, 0115-6811-10
• Packager: Amneal Pharmaceuticals of New York LLC

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BUPROPION HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 42291-182-30, 42291-182-50, 42291-183-30, 42291-183-50
• Packager: AvKARE
• This is a repackaged label.
• Source NDC Code(s): 10370-101, 10370-102

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BUPROPION HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 50268-140-11, 50268-140-13, 50268-141-11, 50268-141-15
• Packager: AvPAK
• This is a repackaged label.
• Source NDC Code(s): 10370-101, 10370-102

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BUPROPION HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 63629-7033-1, 63629-7033-2, 63629-7033-3, 63629-7033-4, view more
63629-7033-5, 63629-7033-6, 63629-7033-7
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 0115-6811

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BUPROPION HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 71335-1156-1, 71335-1156-2, 71335-1156-3, 71335-1156-4, view more
71335-1156-5
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 0115-6811

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BUPROPION HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 63629-2137-1
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 10370-101

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BUPROPION HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 67046-082-07, 67046-082-14, 67046-082-15, 67046-082-20, view more
67046-082-21, 67046-082-28, 67046-082-30, 67046-082-60
• Packager: Contract Pharmacy Services-PA
• This is a repackaged label.
• Source NDC Code(s): 10370-101

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BUPROPION HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 61919-589-30
• Packager: Direct Rx
• This is a repackaged label.
• Source NDC Code(s): 10370-101

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BUPROPION HYDROCHLORIDE tablet, film coated, extended release

NDC Code(s): 61919-589-60
• Packager: Direct_Rx
• This is a repackaged label.
• Source NDC Code(s): 10370-101