dok

Generic: docusate sodium

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

Drug Facts

Product Profile

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

docusate sodium 100 mg/1

Manufacturer
MAJOR PHARMACEUTICALS

Identifiers & Regulatory

Product NDC 0904-6750
Product ID 0904-6750_08649f2e-5f6c-5ba0-e063-6294a90a5fd1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2018-06-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046750
Hyphenated Format 0904-6750

Supplemental Identifiers

RxCUI
1099279 1483574
UPC
0309046750604
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 dok (source: ndc)
Generic Name docusate sodium (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0904-6750-60)
source: ndc

Packages (1)

0904-6750-60 100 TABLET in 1 BOTTLE (0904-6750-60)

Ingredients (1)

docusate sodium (100 mg/1)

Linked Drug Pages (1)

DOK ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "08649f2e-5f6c-5ba0-e063-6294a90a5fd1", "openfda": {"upc": ["0309046750604"], "unii": ["F05Q2T2JA0"], "rxcui": ["1099279", "1483574"], "spl_set_id": ["7a92070d-98cc-662f-e053-2991aa0aa1b2"], "manufacturer_name": ["MAJOR PHARMACEUTICALS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0904-6750-60)", "package_ndc": "0904-6750-60", "marketing_start_date": "20180601"}], "brand_name": "DOK", "product_id": "0904-6750_08649f2e-5f6c-5ba0-e063-6294a90a5fd1", "dosage_form": "TABLET", "product_ndc": "0904-6750", "generic_name": "docusate sodium", "labeler_name": "MAJOR PHARMACEUTICALS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DOK", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "100 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180601", "listing_expiration_date": "20261231"}