Package 10202-722-05

Brand: acid reducer

Generic: omeprazole
NDC Package

Package Facts

Identity

Package NDC 10202-722-05
Digits Only 1020272205
Product NDC 10202-722
Description

1 BOTTLE in 1 CARTON (10202-722-05) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-06-06
Brand acid reducer
Generic omeprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d9c2719b-9650-41da-8ad4-085852934eeb", "openfda": {"upc": ["0052548690663"], "unii": ["426QFE7XLK"], "rxcui": ["402014"], "spl_set_id": ["61206416-e0c1-44d7-ad35-feb629361ba9"], "manufacturer_name": ["7-Eleven"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (10202-722-05)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "10202-722-05", "marketing_start_date": "20180606"}], "brand_name": "Acid Reducer", "product_id": "10202-722_d9c2719b-9650-41da-8ad4-085852934eeb", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "10202-722", "generic_name": "Omeprazole", "labeler_name": "7-Eleven", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acid Reducer", "active_ingredients": [{"name": "OMEPRAZOLE MAGNESIUM", "strength": "20 mg/1"}], "application_number": "ANDA206877", "marketing_category": "ANDA", "marketing_start_date": "20180606", "listing_expiration_date": "20261231"}