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United States · US · US:63187-012_c9045cc9-47f1-4fe5-88fe-63edeb985739
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 · 5
- ndc1163187012066 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-012-06)
- ndc11631870121515 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-012-15)
- ndc11631870122020 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-012-20)
- ndc11631870123030 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-012-30)
- ndc11631870126060 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-012-60)
Annotations
UNII (FDA Substance ID)
QTG126297Q
DICLOFENAC SODIUM
RxCUI 203214
Orange Book
A077863
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": "ORAL",
"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": "63187-012_c9045cc9-47f1-4fe5-88fe-63edeb985739",
"productndc": "63187-012",
"dosage_form": "TABLET, DELAYED RELEASE",
"orange_book": {
"appl_no": "077863",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "75MG",
"product_no": "003",
"approval_date": "Jun 8, 2007"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DICLOFENAC SODIUM",
"proprietary_name": "Diclofenac Sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA077863",
"marketing_category": "ANDA",
"nonproprietary_name": "Diclofenac Sodium",
"start_marketing_date": "20080819",
"active_numerator_strength": "75"
}Related drugs
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