docusate sodium

Generic: docusate sodium

Labeler: major pharmaceuticals
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name docusate sodium
Generic Name docusate sodium
Labeler major pharmaceuticals
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

docusate sodium 100 mg/10mL

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7279
Product ID 0904-7279_ac88d5b7-192e-456b-ae3e-3813294d4617
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2022-12-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047279
Hyphenated Format 0904-7279

Supplemental Identifiers

RxCUI
1245686
UNII
F05Q2T2JA0

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name docusate sodium (source: ndc)
Generic Name docusate sodium (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/10mL
source: ndc
Packaging
  • 10 TRAY in 1 CASE (0904-7279-72) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0904-7279-66)
source: ndc

Packages (1)

Ingredients (1)

docusate sodium (100 mg/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ac88d5b7-192e-456b-ae3e-3813294d4617", "openfda": {"unii": ["F05Q2T2JA0"], "rxcui": ["1245686"], "spl_set_id": ["1541ff5b-11f8-444b-a2a0-8e3086ae650a"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (0904-7279-72)  / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0904-7279-66)", "package_ndc": "0904-7279-72", "marketing_start_date": "20221208"}], "brand_name": "Docusate Sodium", "product_id": "0904-7279_ac88d5b7-192e-456b-ae3e-3813294d4617", "dosage_form": "LIQUID", "product_ndc": "0904-7279", "generic_name": "Docusate Sodium", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Docusate Sodium", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "100 mg/10mL"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221208", "listing_expiration_date": "20261231"}