NDC 70518-1885

Sennosides,Docusate sodium

Sennosides,docusate Sodium

Sennosides,Docusate sodium is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Docusate Sodium; Sennosides.

• Product ID: 70518-1885_82837451-6d69-2197-e053-2991aa0aa80a
• NDC: 70518-1885
• Product Type: Human Otc Drug
• Proprietary Name: Sennosides,Docusate sodium
• Generic Name: Sennosides,docusate Sodium
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2019-02-20
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part334
• Labeler Name: REMEDYREPACK INC.
• 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 70518-1885-0

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1885-0)

• Marketing Start Date: 2019-02-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70518-1885-0 [70518188500]

Sennosides,Docusate sodium TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part334
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-02-20

Drug Details

Active Ingredients

Ingredient	Strength
DOCUSATE SODIUM	50 mg/1

OpenFDA Data

• SPL SET ID: 0ac06b43-8a99-4681-8a03-1f26b3326776
• Manufacturer:
  • REMEDYREPACK INC.
• UNII:
  • F05Q2T2JA0
  • 3FYP5M0IJX
• RxNorm Concept Unique ID - RxCUI:
  • 998740

NDC Crossover Matching brand name "Sennosides,Docusate sodium" or generic name "Sennosides,docusate Sodium"

NDC	Brand Name	Generic Name
0536-1169	Sennosides,Docusate sodium	Sennosides,Docusate sodium
0615-8276	Sennosides,Docusate sodium	Sennosides,Docusate sodium
0904-6724	Sennosides,Docusate sodium	Sennosides,Docusate sodium
55154-7299	Sennosides,Docusate sodium	Sennosides,Docusate sodium
70518-1885	Sennosides,Docusate sodium	Sennosides,Docusate sodium