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United States · US · US:50090-2454_98e8ede7-aa2f-4dfa-90de-b7a9c5b828b4
Diclofenac Sodium
Orange BookUNIISPLATC M01AB55
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeM01AB55
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1150090245401 BOTTLE, DROPPER in 1 CARTON (50090-2454-0) / 5 mL in 1 BOTTLE, DROPPER
Annotations
UNII (FDA Substance ID)
QTG126297Q
DICLOFENAC SODIUM
RxCUI 203214
Orange Book
A078792
AT
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": "OPHTHALMIC",
"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": "50090-2454_98e8ede7-aa2f-4dfa-90de-b7a9c5b828b4",
"productndc": "50090-2454",
"dosage_form": "SOLUTION/ DROPS",
"orange_book": {
"appl_no": "078792",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AT",
"strength": "0.1%",
"product_no": "001",
"approval_date": "Dec 28, 2007"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DICLOFENAC SODIUM",
"proprietary_name": "Diclofenac Sodium",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA078792",
"marketing_category": "ANDA",
"nonproprietary_name": "Diclofenac Sodium",
"start_marketing_date": "20071228",
"active_numerator_strength": "1"
}Related drugs
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