NDC 55154-0733

DOK Plus

Dok Plus

DOK Plus is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Cardinal Health. The primary component is Docusate Sodium; Sennosides.

• Product ID: 55154-0733_5eccc116-10e4-40b3-84e7-9e29787e949d
• NDC: 55154-0733
• Product Type: Human Otc Drug
• Proprietary Name: DOK Plus
• Generic Name: Dok Plus
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2011-06-07
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part334
• Labeler Name: Cardinal Health
• Substance Name: DOCUSATE SODIUM; SENNOSIDES
• Active Ingredient Strength: 50 mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 55154-0733-0

10 BLISTER PACK in 1 BAG (55154-0733-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

• Marketing Start Date: 2011-06-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55154-0733-0 [55154073300]

DOK Plus TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part334
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-06-07

Drug Details

Active Ingredients

Ingredient	Strength
DOCUSATE SODIUM	50 mg/1

OpenFDA Data

• SPL SET ID: 8bb66fe4-e216-4fc2-b91c-500ded0a9624
• Manufacturer:
  • Cardinal Health
• UNII:
  • F05Q2T2JA0
  • 3FYP5M0IJX
• RxNorm Concept Unique ID - RxCUI:
  • 998740
• UPC Code:
  • 0055154073301