Package 71205-613-60

Brand: omeprazole

Generic: omeprazole
NDC Package

Package Facts

Identity

Package NDC 71205-613-60
Digits Only 7120561360
Product NDC 71205-613
Description

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-613-60)

Marketing

Marketing Status
Marketed Since 2021-10-25
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": "d870bdc1-5e26-4153-89e2-f629fef60ad0", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "upc": ["0371205613303"], "unii": ["KG60484QX9"], "rxcui": ["198051"], "spl_set_id": ["13b379ef-7982-434d-9e6b-e01cd2b398d2"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-613-06)", "package_ndc": "71205-613-06", "marketing_start_date": "20230814"}, {"sample": false, "description": "14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-613-14)", "package_ndc": "71205-613-14", "marketing_start_date": "20220307"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-613-30)", "package_ndc": "71205-613-30", "marketing_start_date": "20211025"}, {"sample": false, "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-613-60)", "package_ndc": "71205-613-60", "marketing_start_date": "20211025"}, {"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-613-90)", "package_ndc": "71205-613-90", "marketing_start_date": "20211025"}], "brand_name": "Omeprazole", "product_id": "71205-613_d870bdc1-5e26-4153-89e2-f629fef60ad0", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "71205-613", "generic_name": "Omeprazole", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "20 mg/1"}], "application_number": "ANDA212977", "marketing_category": "ANDA", "marketing_start_date": "20190220", "listing_expiration_date": "20261231"}