laxacin

Generic: docusate sodium and sennosides

Labeler: alexso, inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name laxacin
Generic Name docusate sodium and sennosides
Labeler alexso, inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

docusate sodium 50 mg/1, sennosides a and b 8.6 mg/1

Manufacturer
Alexso, Inc

Identifiers & Regulatory

Product NDC 50488-0901
Product ID 50488-0901_1b45f6d1-4436-4b3a-813b-7043c0d0fad6
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2018-10-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 504880901
Hyphenated Format 50488-0901

Supplemental Identifiers

RxCUI
998740 2106884
UNII
F05Q2T2JA0 1B5FPI42EN

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 laxacin (source: ndc)
Generic Name docusate sodium and sennosides (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
  • 8.6 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50488-0901-1)
source: ndc

Packages (1)

50488-0901-1 100 TABLET in 1 BOTTLE (50488-0901-1)

Ingredients (2)

docusate sodium (50 mg/1) sennosides a and b (8.6 mg/1)

Linked Drug Pages (1)

Laxacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b45f6d1-4436-4b3a-813b-7043c0d0fad6", "openfda": {"unii": ["F05Q2T2JA0", "1B5FPI42EN"], "rxcui": ["998740", "2106884"], "spl_set_id": ["0df9abaf-3997-4dde-8003-ae3d8d07cf39"], "manufacturer_name": ["Alexso, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50488-0901-1)", "package_ndc": "50488-0901-1", "marketing_start_date": "20181015"}], "brand_name": "Laxacin", "product_id": "50488-0901_1b45f6d1-4436-4b3a-813b-7043c0d0fad6", "dosage_form": "TABLET", "product_ndc": "50488-0901", "generic_name": "Docusate sodium and sennosides", "labeler_name": "Alexso, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Laxacin", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/1"}, {"name": "SENNOSIDES A AND B", "strength": "8.6 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20181015", "listing_expiration_date": "20261231"}