Package 57483-740-42

Brand: omeprazole

Generic: omeprazole
NDC Package

Package Facts

Identity

Package NDC 57483-740-42
Digits Only 5748374042
Product NDC 57483-740
Description

3 BOTTLE in 1 CARTON (57483-740-42) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57483-740-01)

Marketing

Marketing Status
Marketed Since 2020-08-06
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": "ce5c9fdc-0c50-4315-8f11-e00c9810abd0", "openfda": {"unii": ["426QFE7XLK"], "rxcui": ["198051"], "spl_set_id": ["ce5c9fdc-0c50-4315-8f11-e00c9810abd0"], "manufacturer_name": ["INNOVUS PHARMACEUTICALS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BOTTLE in 1 CARTON (57483-740-42)  / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57483-740-01)", "package_ndc": "57483-740-42", "marketing_start_date": "20200806"}], "brand_name": "omeprazole", "product_id": "57483-740_ce5c9fdc-0c50-4315-8f11-e00c9810abd0", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "57483-740", "generic_name": "omeprazole", "labeler_name": "INNOVUS PHARMACEUTICALS, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE MAGNESIUM", "strength": "20.6 mg/1"}], "application_number": "ANDA210593", "marketing_category": "ANDA", "marketing_start_date": "20200806", "listing_expiration_date": "20261231"}