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United States · US · US:43063-848_2fc3b270-b101-5a08-e063-6394a90a7fd2
Diclofenac Potassium
Orange BookUNIISPLATC M01AB55
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPD-Rx Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeM01AB55
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11430638482121 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-848-21)
- ndc11430638483030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-848-30)
Annotations
UNII (FDA Substance ID)
L4D5UA6CB4
DICLOFENAC POTASSIUM
RxCUI 81997
Orange Book
A075219
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "L4D5UA6CB4",
"rxcui": "81997",
"inchikey": "KXZOIWWTXOCYKR-UHFFFAOYSA-M",
"display_name": "DICLOFENAC POTASSIUM",
"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": "43063-848_2fc3b270-b101-5a08-e063-6394a90a7fd2",
"productndc": "43063-848",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "075219",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG",
"product_no": "001",
"approval_date": "Aug 6, 1998"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DICLOFENAC POTASSIUM",
"proprietary_name": "Diclofenac Potassium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075219",
"marketing_category": "ANDA",
"nonproprietary_name": "Diclofenac Potassium",
"start_marketing_date": "19980811",
"active_numerator_strength": "50"
}Related drugs
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