diazoxide

Generic: diazoxide

Labeler: e5 pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diazoxide
Generic Name diazoxide
Labeler e5 pharma, llc
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

diazoxide 50 mg/mL

Manufacturer
e5 Pharma, LLC

Identifiers & Regulatory

Product NDC 13517-100
Product ID 13517-100_11c83c92-145b-486a-90f3-d759c358d091
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211050
Listing Expiration 2026-12-31
Marketing Start 2019-12-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 13517100
Hyphenated Format 13517-100

Supplemental Identifiers

RxCUI
197593
UPC
0313517100300
UNII
O5CB12L4FN

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name diazoxide (source: ndc)
Generic Name diazoxide (source: ndc)
Application Number ANDA211050 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (13517-100-30) / 30 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (1)

13517-100-30 1 BOTTLE, DROPPER in 1 CARTON (13517-100-30) / 30 mL in 1 BOTTLE, DROPPER

Ingredients (1)

diazoxide (50 mg/mL)

Linked Drug Pages (1)

Diazoxide ndc-match (0.9)

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"}