docusate sodium, extra strength 250 mg
Generic: docusate sodium
Labeler: advanced rx llcDrug 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
Active Ingredients
docusate sodium 250 mg/1
Manufacturer
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
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 100 CAPSULE, GELATIN COATED in 1 BOTTLE (80513-100-01)
Packages (1)
Ingredients (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"}