SEARCH RESULTS for: 310346 [RxCUI] (58 results)

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FINASTERIDE tablet, film coated

NDC Code(s): 68788-8377-1, 68788-8377-3, 68788-8377-6, 68788-8377-9
• Packager: Preferred Pharmaceuticals, Inc.
• This is a repackaged label.
• Source NDC Code(s): 31722-525

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FINASTERIDE tablet, film coated

NDC Code(s): 63187-265-10, 63187-265-30, 63187-265-60, 63187-265-90
• Packager: Proficient Rx LP
• This is a repackaged label.
• Source NDC Code(s): 16729-090

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FINASTERIDE tablet, film coated

NDC Code(s): 71205-767-30, 71205-767-60, 71205-767-90
• Packager: Proficient Rx LP
• This is a repackaged label.
• Source NDC Code(s): 67877-288

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FINASTERIDE tablet, film coated

NDC Code(s): 82009-061-05
• Packager: QUALLENT PHARMACEUTICALS HEALTH LLC

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FINASTERIDE tablet, film coated

NDC Code(s): 70518-0397-0, 70518-0397-1, 70518-0397-2
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 16729-090

• 

FINASTERIDE tablet, film coated

NDC Code(s): 70518-2363-0, 70518-2363-1, 70518-2363-2, 70518-2363-3, view more
70518-2363-4, 70518-2363-5
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 16729-090

• 

FINASTERIDE tablet, film coated

NDC Code(s): 70518-1704-0, 70518-1704-1
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 57237-062

• 

FINASTERIDE tablet, film coated

NDC Code(s): 70518-3182-0, 70518-3182-1, 70518-3182-2, 70518-3182-3
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 31722-525

• 

FINASTERIDE tablet, film coated

NDC Code(s): 70518-3612-0, 70518-3612-1
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 0093-7355

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FINASTERIDE tablet, film coated

NDC Code(s): 70518-3600-0, 70518-3600-1, 70518-3600-2, 70518-3600-3
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 67877-288

• 

FINASTERIDE tablet, film coated

NDC Code(s): 70518-3616-0, 70518-3616-1, 70518-3616-2, 70518-3616-3, view more
70518-3616-4
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 65862-149

• 

FINASTERIDE tablet, film coated

NDC Code(s): 57237-062-05, 57237-062-30, 57237-062-90
• Packager: Rising Pharma Holdings, Inc.

• 

FINASTERIDE tablet, film coated

NDC Code(s): 47335-715-08, 47335-715-13, 47335-715-18, 47335-715-81, view more
47335-715-83, 47335-715-88
• Packager: Sun Pharmaceutical Industries, Inc.

• 

FINASTERIDE tablet, film coated

NDC Code(s): 0093-7355-05, 0093-7355-56, 0093-7355-98
• Packager: Teva Pharmaceuticals USA, Inc.

• 

FINASTERIDE tablet, film coated

NDC Code(s): 70771-1152-0, 70771-1152-1, 70771-1152-3, 70771-1152-4
• Packager: Zydus Lifesciences Limited

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FINASTERIDE tablet, film coated

NDC Code(s): 68382-074-01, 68382-074-06, 68382-074-10, 68382-074-77
• Packager: Zydus Pharmaceuticals USA Inc.

• 

FINASTERIDE tablet

NDC Code(s): 65977-5025-0, 65977-5025-1, 65977-5025-2, 65977-5025-3, view more
65977-5025-4
• Packager: Hetero Drugs Limited

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PROSCAR (finasteride) tablet, film coated

NDC Code(s): 78206-153-01, 78206-153-02
• Packager: Organon LLC