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United States · US · US:82804-052_f19bf286-f4dd-4491-90c3-9f8713071903
DICLOFENAC SODIUM
Orange BookUNIISPLATC M01AB55
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeM01AB55
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1182804052001 TUBE in 1 CARTON (82804-052-00) / 100 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
QTG126297Q
DICLOFENAC SODIUM
RxCUI 203214
Orange Book
A208301
AB
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": "82804-052_f19bf286-f4dd-4491-90c3-9f8713071903",
"productndc": "82804-052",
"dosage_form": "GEL",
"orange_book": {
"appl_no": "208301",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "3%",
"product_no": "001",
"approval_date": "Sep 13, 2016"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DICLOFENAC SODIUM",
"proprietary_name": "DICLOFENAC SODIUM",
"active_ingred_unit": "mg/g",
"application_number": "ANDA208301",
"marketing_category": "ANDA",
"nonproprietary_name": "diclofenac sodium",
"start_marketing_date": "20160913",
"active_numerator_strength": "30"
}Related drugs
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