Package 71399-0027-8

Brand: onelax senna

Generic: senna
NDC Package

Package Facts

Identity

Package NDC 71399-0027-8
Digits Only 7139900278
Product NDC 71399-0027
Product ID 71399-0027_4227fa19-b935-0fbc-e063-6294a90ac342
Description

237 mL in 1 BOTTLE (71399-0027-8)

Marketing

Marketing Status
Marketed Since 2024-02-06
Brand onelax senna
Generic senna
Sample Package No

Linked Drug Pages (1)

OneLAX SENNA ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4227fa19-b935-0fbc-e063-6294a90ac342", "openfda": {"upc": ["0371399002785"], "unii": ["1B5FPI42EN"], "rxcui": ["702311"], "spl_set_id": ["27fa8f54-ed84-4afd-8da3-8754da48643b"], "manufacturer_name": ["Akron Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (71399-0027-8)", "package_ndc": "71399-0027-8", "marketing_start_date": "20240206"}], "brand_name": "OneLAX SENNA", "product_id": "71399-0027_4227fa19-b935-0fbc-e063-6294a90ac342", "dosage_form": "SYRUP", "product_ndc": "71399-0027", "generic_name": "SENNA", "labeler_name": "Akron Pharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "OneLAX SENNA", "active_ingredients": [{"name": "SENNOSIDES A AND B", "strength": "417.12 mg/237mL"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240206", "listing_expiration_date": "20261231"}