Package 62175-136-37
Brand: omeprazole
Generic: omeprazolePackage Facts
Identity
Package NDC
62175-136-37
Digits Only
6217513637
Product NDC
62175-136
Description
100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-37)
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": "e786b865-dc62-4018-9cb1-7056b7ca2cde", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "upc": ["0362175136329", "0362175114327", "0362175118325"], "unii": ["KG60484QX9"], "rxcui": ["198051", "199119", "200329"], "spl_set_id": ["92201fb1-4570-42db-8da3-3b8c0e291d32"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-32)", "package_ndc": "62175-136-32", "marketing_start_date": "20090123"}, {"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-37)", "package_ndc": "62175-136-37", "marketing_start_date": "20090123"}, {"sample": false, "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-43)", "package_ndc": "62175-136-43", "marketing_start_date": "20090123"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-46)", "package_ndc": "62175-136-46", "marketing_start_date": "20090123"}, {"sample": false, "description": "36000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-136-49)", "package_ndc": "62175-136-49", "marketing_start_date": "20090123"}], "brand_name": "Omeprazole", "product_id": "62175-136_e786b865-dc62-4018-9cb1-7056b7ca2cde", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "62175-136", "generic_name": "omeprazole", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "40 mg/1"}], "application_number": "ANDA075410", "marketing_category": "ANDA", "marketing_start_date": "20090123", "listing_expiration_date": "20261231"}