docu liquid

Generic: docusate sodium

Labeler: atlantic biologicals corp.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name docu liquid
Generic Name docusate sodium
Labeler atlantic biologicals corp.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

docusate sodium 50 mg/5mL

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-0771
Product ID 17856-0771_3b3f3045-55db-5ed5-e063-6294a90aab75
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M
Listing Expiration 2026-12-31
Marketing Start 1997-08-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 178560771
Hyphenated Format 17856-0771

Supplemental Identifiers

RxCUI
1248119
UNII
F05Q2T2JA0

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 docu liquid (source: ndc)
Generic Name docusate sodium (source: ndc)
Application Number M (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/5mL
source: ndc
Packaging
  • Package/Label Principal Display Panel image 1 image 2
source: label

Packages (0)

No package records.

Ingredients (1)

docusate sodium (50 mg/5mL)

Linked Drug Pages (1)

Docu Liquid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b3f3045-55db-5ed5-e063-6294a90aab75", "openfda": {"unii": ["F05Q2T2JA0"], "rxcui": ["1248119"], "spl_set_id": ["f4ed0721-3be9-4108-a6c9-dbbe115249e9"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [], "brand_name": "Docu Liquid", "product_id": "17856-0771_3b3f3045-55db-5ed5-e063-6294a90aab75", "dosage_form": "LIQUID", "product_ndc": "17856-0771", "generic_name": "Docusate Sodium", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Docu Liquid", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/5mL"}], "application_number": "M", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19970801", "listing_expiration_date": "20261231"}