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United States · US · US:70954-668_9732cf08-dad4-42a4-a10e-0284848724d7
Pentoxifylline
Orange BookUNIISPLATC C04AD03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerANI Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeC04AD03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc117095466810100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70954-668-10)
- ndc117095466820500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70954-668-20)
Annotations
UNII (FDA Substance ID)
SD6QCT3TSU
PENTOXIFYLLINE
RxCUI 8013
Orange Book
A074878
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "SD6QCT3TSU",
"rxcui": "8013",
"inchikey": "BYPFEZZEUUWMEJ-UHFFFAOYSA-N",
"display_name": "PENTOXIFYLLINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"08b095b6-be53-41f5-a284-fe15d4852f79": {
"match": "brand_token",
"title": "PENTOXIFYLLINE POWDER [AX PHARMACEUTICAL CORP]",
"spl_version": "3",
"published_date": "2026-03-12"
}
},
"productid": "70954-668_9732cf08-dad4-42a4-a10e-0284848724d7",
"productndc": "70954-668",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "074878",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "400MG",
"product_no": "001",
"approval_date": "Jul 9, 1997"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PENTOXIFYLLINE",
"proprietary_name": "Pentoxifylline",
"active_ingred_unit": "mg/1",
"application_number": "ANDA074878",
"marketing_category": "ANDA",
"nonproprietary_name": "Pentoxifylline",
"start_marketing_date": "20240115",
"active_numerator_strength": "400"
}Related drugs
Other records sharing ATC code C04AD03.
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