NDC 42787-105

SENOKOT-S

Docuset Sodium

SENOKOT-S is a Oral Pill in the Human Otc Drug category. It is labeled and distributed by Ajes Pharmaceuticals,llc. The primary component is Docusate Sodium; Sennosides.

• Product ID: 42787-105_6558ce50-cba7-464e-9cad-a0206629c2ef
• NDC: 42787-105
• Product Type: Human Otc Drug
• Proprietary Name: SENOKOT-S
• Generic Name: Docuset Sodium
• Dosage Form: Pill
• Route of Administration: ORAL
• Marketing Start Date: 2012-09-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part334
• Labeler Name: Ajes Pharmaceuticals,LLC
• Substance Name: DOCUSATE SODIUM; SENNOSIDES
• Active Ingredient Strength: 50 mg/340mg; mg/340mg
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 42787-105-12

1 BOTTLE in 1 BOX (42787-105-12) > 50000 mg in 1 BOTTLE

• Marketing Start Date: 2012-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 42787-105-12 [42787010512]

SENOKOT-S PILL

• Marketing Category: OTC monograph not final
• Application Number: part334
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-09-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
DOCUSATE SODIUM	50 mg/340mg

OpenFDA Data

• SPL SET ID: abecc082-4c04-4fae-b8e5-91ddc54d6e0c
• Manufacturer:
  • Ajes Pharmaceuticals,LLC
• UNII:
  • F05Q2T2JA0
  • 3FYP5M0IJX

NDC Crossover Matching brand name "SENOKOT-S" or generic name "Docuset Sodium"

NDC	Brand Name	Generic Name
42787-105	SENOKOT-S	Docuset Sodium
67618-310	Senokot-S	standardized senna concentrate and docusate sodium