Package 72789-352-30
Brand: esomeprazole magnesium
Generic: esomeprazole magnesiumPackage Facts
Identity
Package NDC
72789-352-30
Digits Only
7278935230
Product NDC
72789-352
Description
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-352-30)
Marketing
Marketing Status
Brand
esomeprazole magnesium
Generic
esomeprazole magnesium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38063934-d3b6-c6af-e063-6294a90a853c", "openfda": {"upc": ["0372789352305"], "unii": ["36H71644EQ"], "rxcui": ["606726"], "spl_set_id": ["ac12cd05-10cf-4694-a9e8-e5f04fe162a7"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-352-30)", "package_ndc": "72789-352-30", "marketing_start_date": "20231009"}], "brand_name": "Esomeprazole Magnesium", "product_id": "72789-352_38063934-d3b6-c6af-e063-6294a90a853c", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72789-352", "generic_name": "Esomeprazole Magnesium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Esomeprazole Magnesium", "active_ingredients": [{"name": "ESOMEPRAZOLE MAGNESIUM DIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA205606", "marketing_category": "ANDA", "marketing_start_date": "20160421", "listing_expiration_date": "20261231"}