SEARCH RESULTS for: 577033 [RxCUI] (84 results)

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REVATIO (sildenafil citrate) tablet, film coated
REVATIO (sildenafil citrate) injection, solution
REVATIO (sildenafil citrate) powder, for suspension

NDC Code(s): 0069-0336-21, 0069-0338-01, 0069-4190-68
• Packager: PFIZER LABORATORIES DIV PFIZER INC

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REVATIO (sildenafil citrate) tablet, film coated
REVATIO (sildenafil citrate) injection, solution
REVATIO (sildenafil citrate) powder, for suspension

NDC Code(s): 58151-385-35, 58151-395-31, 58151-402-77
• Packager: Viatris Specialty LLC

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SILDENAFIL CITRATE (sildenafil) tablet, film coated

NDC Code(s): 72888-018-00, 72888-018-90
• Packager: Advagen Pharma Ltd

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SILDENAFIL CITRATE (sildenafil) tablet, film coated

NDC Code(s): 17856-8100-1, 17856-8100-2, 17856-8100-3, 17856-8100-4, view more
17856-8100-5
• Packager: ATLANTIC BIOLOGICALS CORP.
• This is a repackaged label.
• Source NDC Code(s): 52817-295

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SILDENAFIL CITRATE (sildenafil) tablet, film coated

NDC Code(s): 51655-793-20, 51655-793-52
• Packager: Northwind Health Company, LLC
• This is a repackaged label.
• Source NDC Code(s): 52817-295

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SILDENAFIL CITRATE (sildenafil) tablet, film coated

NDC Code(s): 82868-094-30
• Packager: Northwind Health Company, LLC
• This is a repackaged label.
• Source NDC Code(s): 72888-018

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SILDENAFIL CITRATE (sildenafil) tablet, film coated

NDC Code(s): 71205-305-10, 71205-305-20, 71205-305-30, 71205-305-60, view more
71205-305-90
• Packager: Proficient Rx LP
• This is a repackaged label.
• Source NDC Code(s): 52817-295

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SILDENAFIL CITRATE (sildenafil) tablet, film coated

NDC Code(s): 71205-623-10, 71205-623-30, 71205-623-60, 71205-623-90
• Packager: Proficient Rx LP
• This is a repackaged label.
• Source NDC Code(s): 72888-018

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SILDENAFIL CITRATE (sildenafil) tablet, film coated

NDC Code(s): 67296-1488-9
• Packager: RedPharm Drug Inc
• This is a repackaged label.
• Source NDC Code(s): 52817-295

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SILDENAFIL CITRATE (sildenafil) tablet, film coated

NDC Code(s): 52817-295-00, 52817-295-90
• Packager: TruPharma LLC

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SILDENAFIL CITRATE (sildenafil) tablet, film coated

NDC Code(s): 50436-0295-1, 50436-0295-2, 50436-0295-3, 50436-0295-4, view more
50436-0295-5
• Packager: Unit Dose Services
• This is a repackaged label.
• Source NDC Code(s): 52817-295

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SILDENAFIL CITRATE (sildenafil) tablet, film coated

NDC Code(s): 50436-0005-1, 50436-0005-2, 50436-0005-3, 50436-0005-4, view more
50436-0005-5
• Packager: Unit Dose Services
• This is a repackaged label.
• Source NDC Code(s): 42543-005

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SILDENAFIL CITRATE (sildenafil) tablet, film coated

NDC Code(s): 42543-005-10, 42543-005-90
• Packager: Vensun Pharmaceuticals, Inc.

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SILDENAFIL CITRATE tablet

NDC Code(s): 80425-0304-1, 80425-0304-2, 80425-0304-3, 80425-0304-4
• Packager: Advanced Rx Pharmacy of Tennessee, LLC
• This is a repackaged label.
• Source NDC Code(s): 13668-185

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SILDENAFIL CITRATE tablet

NDC Code(s): 76420-613-30, 76420-613-60, 76420-613-90
• Packager: Asclemed USA, Inc.
• This is a repackaged label.
• Source NDC Code(s): 13668-185

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SILDENAFIL CITRATE tablet

NDC Code(s): 50090-3905-0, 50090-3905-1
• Packager: A-S Medication Solutions
• This is a repackaged label.
• Source NDC Code(s): 13668-185

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SILDENAFIL CITRATE tablet

NDC Code(s): 50436-0185-1, 50436-0185-2, 50436-0185-3
• Packager: Unit Dose Services
• This is a repackaged label.
• Source NDC Code(s): 13668-185

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SILDENAFIL (sildenafil citrate) tablet, film coated

NDC Code(s): 68788-7379-3, 68788-7379-4, 68788-7379-6, 68788-7379-9
• Packager: Preferred Pharmaceuticals Inc.
• This is a repackaged label.
• Source NDC Code(s): 0591-3780

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SILDENAFIL (sildenafil citrate) tablet, film coated

NDC Code(s): 50436-0033-1, 50436-0033-2, 50436-0033-3, 50436-0033-4, view more
50436-0033-5
• Packager: Unit Dose Services
• This is a repackaged label.
• Source NDC Code(s): 59762-0033

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SILDENAFIL (sildenafil) tablet, film coated

NDC Code(s): 71335-1649-0, 71335-1649-1, 71335-1649-2, 71335-1649-3, view more
71335-1649-4, 71335-1649-5, 71335-1649-6, 71335-1649-7, 71335-1649-8, 71335-1649-9
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 31722-776