Package 13517-100-30
Brand: diazoxide
Generic: diazoxidePackage Facts
Identity
Package NDC
13517-100-30
Digits Only
1351710030
Product NDC
13517-100
Description
1 BOTTLE, DROPPER in 1 CARTON (13517-100-30) / 30 mL in 1 BOTTLE, DROPPER
Marketing
Marketing Status
Brand
diazoxide
Generic
diazoxide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "11c83c92-145b-486a-90f3-d759c358d091", "openfda": {"upc": ["0313517100300"], "unii": ["O5CB12L4FN"], "rxcui": ["197593"], "spl_set_id": ["c0237320-2d3f-4907-a4d3-08f138aa4ca8"], "manufacturer_name": ["e5 Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (13517-100-30) / 30 mL in 1 BOTTLE, DROPPER", "package_ndc": "13517-100-30", "marketing_start_date": "20191211"}], "brand_name": "Diazoxide", "product_id": "13517-100_11c83c92-145b-486a-90f3-d759c358d091", "dosage_form": "SUSPENSION", "product_ndc": "13517-100", "generic_name": "diazoxide", "labeler_name": "e5 Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazoxide", "active_ingredients": [{"name": "DIAZOXIDE", "strength": "50 mg/mL"}], "application_number": "ANDA211050", "marketing_category": "ANDA", "marketing_start_date": "20191211", "listing_expiration_date": "20261231"}