Package 58602-837-05

Brand: omeprazole

Generic: omeprazole
NDC Package

Package Facts

Identity

Package NDC 58602-837-05
Digits Only 5860283705
Product NDC 58602-837
Description

1 BOTTLE in 1 CARTON (58602-837-05) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-04-28
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": "0c2600f3-e9de-4e73-8ee1-9aeb94d228e4", "openfda": {"upc": ["0358602837051"], "unii": ["426QFE7XLK"], "rxcui": ["198051"], "spl_set_id": ["19097902-a5e6-423a-8569-31c569cd3cdb"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-837-05)  / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "58602-837-05", "marketing_start_date": "20230428"}], "brand_name": "Omeprazole", "product_id": "58602-837_0c2600f3-e9de-4e73-8ee1-9aeb94d228e4", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "58602-837", "generic_name": "Omeprazole", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE MAGNESIUM", "strength": "20 mg/1"}], "application_number": "ANDA213201", "marketing_category": "ANDA", "marketing_start_date": "20230428", "listing_expiration_date": "20261231"}