Laxa-basic 100
Generic: Docusate Sodium
Labeler: BASIC DRUGS, INC.Drug Facts
Product Profile
Brand Name
Laxa-basic 100
Generic Name
Docusate Sodium
Labeler
BASIC DRUGS, INC.
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
DOCUSATE SODIUM 100 mg/1
Identifiers & Regulatory
Product NDC
0761-0434
Product ID
0761-0434_4525bb51-0edc-eb63-e063-6394a90a485e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Marketing Start
2021-01-01
Marketing End
2026-02-28
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07610434
Hyphenated Format
0761-0434
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
Laxa-basic 100 (source: ndc)
Generic Name
Docusate Sodium (source: ndc)
Application Number
M007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0761-0434-20)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4525bb51-0edc-eb63-e063-6394a90a485e", "openfda": {"upc": ["0307610414204"], "unii": ["F05Q2T2JA0"], "rxcui": ["1115005"], "spl_set_id": ["b8ce1cdd-2c22-1cbd-e053-2a95a90ae05d"], "manufacturer_name": ["BASIC DRUGS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0761-0434-20)", "package_ndc": "0761-0434-20", "marketing_end_date": "20260228", "marketing_start_date": "20210101"}], "brand_name": "Laxa-basic 100", "product_id": "0761-0434_4525bb51-0edc-eb63-e063-6394a90a485e", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "0761-0434", "generic_name": "Docusate Sodium", "labeler_name": "BASIC DRUGS, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Laxa-basic 100", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "100 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260228", "marketing_start_date": "20210101"}