SEARCH RESULTS for: 993541 [RxCUI] (107 results)

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 72189-057-30, 72189-057-60, 72189-124-30, 72189-124-72, view more
72189-134-30, 72189-134-60, 72189-134-72, 72189-134-90
• Packager: DIRECT RX
• This is a repackaged label.
• Source NDC Code(s): 16729-443, 16729-444, 43547-288

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 70010-784-03, 70010-784-05, 70010-784-09, 70010-785-03, view more
70010-785-05, 70010-785-09
• Packager: Granules Pharmaceuticals Inc.

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 76519-1021-3, 76519-1021-5
• Packager: H.J. Harkins Company Inc.

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 45865-975-30, 45865-975-60
• Packager: medsource pharmaceuticals
• This is a repackaged label.
• Source NDC Code(s): 16729-443

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 0615-8504-05, 0615-8504-39, 0615-8505-05, 0615-8505-39
• Packager: NCS HealthCare of KY, LLC dba Vangard Labs
• This is a repackaged label.
• Source NDC Code(s): 16571-862, 16571-863

• 

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

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 68071-2586-9
• Packager: NuCare Pharmaceuticals,Inc.
• This is a repackaged label.
• Source NDC Code(s): 16729-443

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 68071-3559-9
• Packager: NuCare Pharmaceuticals,Inc.
• This is a repackaged label.
• Source NDC Code(s): 68180-319

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 72789-301-90
• Packager: PD-Rx Pharmaceuticals, Inc.
• This is a repackaged label.
• Source NDC Code(s): 16729-443

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 68788-4010-1, 68788-4010-3, 68788-4010-6, 68788-4010-9
• Packager: Preferred Pharmaceuticals Inc.
• This is a repackaged label.
• Source NDC Code(s): 70010-784

• 

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

• 

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

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 70518-4674-0
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 16571-862

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 70518-2022-0, 70518-2022-1, 70518-2022-2
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 68180-319

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 70518-4189-0, 70518-4189-1
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 70010-784

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 70518-2458-0, 70518-2458-1, 70518-2458-2, 70518-2458-3, view more
70518-2458-4, 70518-2458-5, 70518-2458-6, 70518-2458-7
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 16729-443

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 16571-862-03, 16571-862-09, 16571-862-10, 16571-862-12, view more
16571-862-50, 16571-863-03, 16571-863-09, 16571-863-10, 16571-863-50
• Packager: Rising Pharma Holdings, Inc.

• 

BUPROPION HYDROCHLORIDE tablet, extended release

NDC Code(s): 53002-4495-0, 53002-4495-3
• Packager: RPK Pharmaceuticals, Inc.
• This is a repackaged label.
• Source NDC Code(s): 16729-443

• 

BUPROPION HYDROCHLORIDE tablet, extended release

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

• 

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