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United States · US · US:0143-9006_6468455a-a638-4ef0-8bce-41afa7f24c66
AcetaZOLAMIDE
Orange BookUNIISPLATC S01EC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHikma Pharmaceuticals USA Inc.
CountryUS (United States)
ATC codeS01EC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1101439006011 VIAL in 1 CARTON (0143-9006-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Annotations
UNII (FDA Substance ID)
429ZT169UH
ACETAZOLAMIDE SODIUM
RxCUI 91406
Orange Book
A040089
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "429ZT169UH",
"rxcui": "91406",
"inchikey": "MRSXAJAOWWFZJJ-UHFFFAOYSA-M",
"display_name": "ACETAZOLAMIDE SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"c5acf531-ba55-47b7-88db-e5da0206ebf1": {
"match": "brand_token",
"title": "ACETAZOLAMIDE CAPSULE, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS]",
"spl_version": "5",
"published_date": "2026-05-25"
}
},
"productid": "0143-9006_6468455a-a638-4ef0-8bce-41afa7f24c66",
"productndc": "0143-9006",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"orange_book": {
"appl_no": "040089",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 500MG BASE/VIAL",
"product_no": "001",
"approval_date": "Feb 28, 1995"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ACETAZOLAMIDE SODIUM",
"proprietary_name": "AcetaZOLAMIDE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA040089",
"marketing_category": "ANDA",
"nonproprietary_name": "Acetazolamide",
"start_marketing_date": "19960501",
"active_numerator_strength": "500"
}Related drugs
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