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United States · US · US:72189-473_4d3a6fe8-20c4-50fe-e063-6294a90affcf
Diclofenac Sodium Gel
Orange BookUNIISPLATC M01AB55
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDirect_Rx
CountryUS (United States)
ATC codeM01AB55
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1172189473011 g in 1 TUBE (72189-473-01)
Annotations
UNII (FDA Substance ID)
QTG126297Q
DICLOFENAC SODIUM
RxCUI 203214
Orange Book
A212351
BX
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "QTG126297Q",
"rxcui": "203214",
"inchikey": "KPHWPUGNDIVLNH-UHFFFAOYSA-M",
"display_name": "DICLOFENAC SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"86461915-9bc1-43d4-8d92-6eef3e56bd90": {
"match": "brand_token",
"title": "DICLOFENAC POTASSIUM TABLET, COATED [BRYANT RANCH PREPACK]",
"spl_version": "104",
"published_date": "2026-06-01"
}
},
"productid": "72189-473_4d3a6fe8-20c4-50fe-e063-6294a90affcf",
"productndc": "72189-473",
"dosage_form": "GEL",
"orange_book": {
"appl_no": "212351",
"products": [
{
"rs": false,
"rld": false,
"te_code": "BX",
"strength": "3%",
"product_no": "001",
"approval_date": "Jul 27, 2022"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DICLOFENAC SODIUM",
"proprietary_name": "Diclofenac Sodium Gel",
"active_ingred_unit": "mg/g",
"application_number": "ANDA212351",
"marketing_category": "ANDA",
"nonproprietary_name": "Diclofenac Sodium Gel",
"start_marketing_date": "20230519",
"active_numerator_strength": "30"
}Related drugs
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