docusate sodium, extra strength 250 mg

Generic: docusate sodium

Labeler: advanced rx llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name docusate sodium, extra strength 250 mg
Generic Name docusate sodium
Labeler advanced rx llc
Dosage Form CAPSULE, GELATIN COATED
Routes
ORAL
Active Ingredients

docusate sodium 250 mg/1

Manufacturer
Advanced Rx LLC

Identifiers & Regulatory

Product NDC 80513-100
Product ID 80513-100_220d2464-6ee6-10d6-e063-6394a90a4f39
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2022-09-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 80513100
Hyphenated Format 80513-100

Supplemental Identifiers

RxCUI
1245468
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, extra strength 250 mg (source: ndc)
Generic Name docusate sodium (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 CAPSULE, GELATIN COATED in 1 BOTTLE (80513-100-01)
source: ndc

Packages (1)

Ingredients (1)

docusate sodium (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "220d2464-6ee6-10d6-e063-6394a90a4f39", "openfda": {"unii": ["F05Q2T2JA0"], "rxcui": ["1245468"], "spl_set_id": ["e8be12c5-c591-eadd-e053-2a95a90a431b"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, GELATIN COATED in 1 BOTTLE (80513-100-01)", "package_ndc": "80513-100-01", "marketing_start_date": "20220915"}], "brand_name": "DOCUSATE SODIUM, EXTRA STRENGTH 250 MG", "product_id": "80513-100_220d2464-6ee6-10d6-e063-6394a90a4f39", "dosage_form": "CAPSULE, GELATIN COATED", "product_ndc": "80513-100", "generic_name": "DOCUSATE SODIUM", "labeler_name": "Advanced Rx LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DOCUSATE SODIUM, EXTRA STRENGTH", "brand_name_suffix": "250 MG", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "250 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220915", "listing_expiration_date": "20261231"}