diazoxide

Generic: diazoxide

Labeler: par health usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diazoxide
Generic Name diazoxide
Labeler par health usa, llc
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

diazoxide 50 mg/mL

Manufacturer
Par Health USA, LLC

Identifiers & Regulatory

Product NDC 0254-1010
Product ID 0254-1010_ca21c9b7-669a-4f0f-afe0-0b166c13bb98
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210799
Listing Expiration 2026-12-31
Marketing Start 2020-07-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02541010
Hyphenated Format 0254-1010

Supplemental Identifiers

RxCUI
197593
UPC
0302541010198
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 ANDA210799 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (0254-1010-19) / 30 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (1)

0254-1010-19 1 BOTTLE, DROPPER in 1 CARTON (0254-1010-19) / 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": "ca21c9b7-669a-4f0f-afe0-0b166c13bb98", "openfda": {"upc": ["0302541010198"], "unii": ["O5CB12L4FN"], "rxcui": ["197593"], "spl_set_id": ["abe317a5-6c63-469c-89c8-9fedfe859c3d"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (0254-1010-19)  / 30 mL in 1 BOTTLE, DROPPER", "package_ndc": "0254-1010-19", "marketing_start_date": "20200721"}], "brand_name": "Diazoxide", "product_id": "0254-1010_ca21c9b7-669a-4f0f-afe0-0b166c13bb98", "dosage_form": "SUSPENSION", "product_ndc": "0254-1010", "generic_name": "Diazoxide", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazoxide", "active_ingredients": [{"name": "DIAZOXIDE", "strength": "50 mg/mL"}], "application_number": "ANDA210799", "marketing_category": "ANDA", "marketing_start_date": "20200721", "listing_expiration_date": "20261231"}