Package 42799-106-01

Brand: methenamine mandelate

Generic: methenamine mandelate
NDC Package

Package Facts

Identity

Package NDC 42799-106-01
Digits Only 4279910601
Product NDC 42799-106
Product ID 42799-106_03695bb1-8e07-4862-b517-04c39d9abee1
Description

100 TABLET in 1 BOTTLE (42799-106-01)

Marketing

Marketing Status
Marketed Since 2009-12-15
Brand methenamine mandelate
Generic methenamine mandelate
Sample Package No

Linked Drug Pages (1)

Methenamine Mandelate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "03695bb1-8e07-4862-b517-04c39d9abee1", "openfda": {"upc": ["0342799105017", "0342799106014"], "unii": ["695N30CINR"], "rxcui": ["992153", "992184"], "spl_set_id": ["cc299e8a-cf9a-4dc6-b6e6-972141e59296"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42799-106-01)", "package_ndc": "42799-106-01", "marketing_start_date": "20091215"}], "brand_name": "Methenamine Mandelate", "product_id": "42799-106_03695bb1-8e07-4862-b517-04c39d9abee1", "dosage_form": "TABLET", "product_ndc": "42799-106", "generic_name": "Methenamine Mandelate", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methenamine Mandelate", "active_ingredients": [{"name": "METHENAMINE MANDELATE", "strength": "1000 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20091215", "listing_expiration_date": "20271231"}