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United States · US · US:85786-104_3c6d4bb5-eb70-944b-e063-6294a90ae8de
Dr Simi All Day Pain Relief
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerFarmacias De Similares TX LLC
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11857861042424 TABLET, FILM COATED in 1 BOTTLE (85786-104-24)
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A091353
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "9TN87S3A3C",
"rxcui": "142442",
"inchikey": "CDBRNDSHEYLDJV-FVGYRXGTSA-M",
"display_name": "NAPROXEN SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"8abd6d8e-c69e-4374-ace8-d42b2d3e171e": {
"match": "brand_token",
"title": "DR SCHOLLS FUNGAL NAIL CLEAR AND CURE TOLNAFTATE ANTIFUNGAL (TOLNAFTATE) LIQUID [SCHOLL'S WELLNESS COMPANY LLC]",
"spl_version": "4",
"published_date": "2026-05-20"
}
},
"productid": "85786-104_3c6d4bb5-eb70-944b-e063-6294a90ae8de",
"productndc": "85786-104",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "091353",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Sep 20, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "Dr Simi All Day Pain Relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA091353",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen sodium",
"start_marketing_date": "20250817",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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