Package 0363-0915-03
Brand: omeprazole
Generic: omeprazolePackage Facts
Identity
Package NDC
0363-0915-03
Digits Only
0363091503
Product NDC
0363-0915
Description
3 BOTTLE in 1 CARTON (0363-0915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
Marketing
Marketing Status
Brand
omeprazole
Generic
omeprazole
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "364bb6a8-58c8-460d-92db-c25b9eed8d2b", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9"], "rxcui": ["402014"], "spl_set_id": ["30a893d2-198a-4184-81b4-02399324ff29"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-0915-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "0363-0915-01", "marketing_start_date": "20101006"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (0363-0915-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "0363-0915-03", "marketing_start_date": "20110325"}, {"sample": false, "description": "2 CARTON in 1 CARTON (0363-0915-30) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0363-0915-30", "marketing_start_date": "20080227"}, {"sample": false, "description": "3 CARTON in 1 CARTON (0363-0915-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "0363-0915-55", "marketing_start_date": "20080227"}], "brand_name": "omeprazole", "product_id": "0363-0915_364bb6a8-58c8-460d-92db-c25b9eed8d2b", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0363-0915", "generic_name": "Omeprazole", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "20 mg/1"}], "application_number": "NDA022032", "marketing_category": "NDA", "marketing_start_date": "20080227", "listing_expiration_date": "20261231"}