Package 11673-915-03

Brand: up and up omeprazole

Generic: omeprazole
NDC Package

Package Facts

Identity

Package NDC 11673-915-03
Digits Only 1167391503
Product NDC 11673-915
Description

3 BOTTLE in 1 CARTON (11673-915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2013-08-14
Brand up and up omeprazole
Generic omeprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cd15d39d-8e0a-4c39-806a-ff9951f33434", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9"], "rxcui": ["402014"], "spl_set_id": ["2f2b26fe-dbc2-4185-8a27-6b166dd49ba2"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-915-01)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "11673-915-01", "marketing_start_date": "20130813"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (11673-915-03)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "11673-915-03", "marketing_start_date": "20130814"}], "brand_name": "up and up omeprazole", "product_id": "11673-915_cd15d39d-8e0a-4c39-806a-ff9951f33434", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "11673-915", "generic_name": "Omeprazole", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "20 mg/1"}], "application_number": "NDA022032", "marketing_category": "NDA", "marketing_start_date": "20090714", "listing_expiration_date": "20261231"}