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United States · US · US:69197-394_3441a647-8818-4c13-9ba8-6a012e46b508
Naproxen Sodium 220mg
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCommand Brands, LLC
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1169197394241 BOTTLE in 1 CARTON (69197-394-24) / 24 TABLET, COATED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A090545
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": {
"c5146d73-2f34-4dfe-ac29-97071279dc4d": {
"match": "brand_token",
"title": "NAPROXEN SODIUM TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]",
"spl_version": "10",
"published_date": "2026-05-28"
}
},
"productid": "69197-394_3441a647-8818-4c13-9ba8-6a012e46b508",
"productndc": "69197-394",
"dosage_form": "TABLET, COATED",
"orange_book": {
"appl_no": "090545",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Mar 16, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "Naproxen Sodium 220mg",
"active_ingred_unit": "mg/1",
"application_number": "ANDA090545",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium 220mg",
"start_marketing_date": "20141223",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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