Package 59726-740-42

Brand: omeprazole

Generic: omeprazole
NDC Package

Package Facts

Identity

Package NDC 59726-740-42
Digits Only 5972674042
Product NDC 59726-740
Description

3 BOTTLE, PLASTIC in 1 BOX (59726-740-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2025-08-15
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": "d1b27e2d-8ea9-4871-bfa2-89463ae0dee0", "openfda": {"unii": ["426QFE7XLK"], "rxcui": ["402014"], "spl_set_id": ["911a08c4-ba73-4600-a5f2-7f26ba8c8604"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BOTTLE, PLASTIC in 1 BOX (59726-740-42)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "59726-740-42", "marketing_start_date": "20250815"}], "brand_name": "Omeprazole", "product_id": "59726-740_d1b27e2d-8ea9-4871-bfa2-89463ae0dee0", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "59726-740", "generic_name": "Omeprazole", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE MAGNESIUM", "strength": "20 mg/1"}], "application_number": "ANDA206582", "marketing_category": "ANDA", "marketing_start_date": "20250815", "listing_expiration_date": "20261231"}