🇺🇸
United States · US · US:71335-0456_824033ce-a50b-4914-b0b9-b0005739555c
Diclofenac Sodium
Orange BookUNIISPLATC M01AB55
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeM01AB55
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 10
- ndc11713350456040 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-0)
- ndc11713350456128 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-1)
- ndc11713350456260 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-2)
- ndc11713350456320 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-3)
- ndc11713350456430 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-4)
- ndc117133504565120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-5)
- ndc11713350456690 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-6)
- ndc117133504567100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-7)
- ndc11713350456815 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-8)
- ndc11713350456914 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-9)
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": "71335-0456_824033ce-a50b-4914-b0b9-b0005739555c",
"productndc": "71335-0456",
"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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