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United States · US · US:69168-394_f6b88aa9-7608-49e8-9841-2cf702715869
Naproxen Caplets
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllegiant Health
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1169168394241 BOTTLE in 1 CARTON (69168-394-24) / 24 TABLET 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": "69168-394_f6b88aa9-7608-49e8-9841-2cf702715869",
"productndc": "69168-394",
"dosage_form": "TABLET",
"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 Caplets",
"active_ingred_unit": "mg/1",
"application_number": "ANDA090545",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium 220 mg",
"start_marketing_date": "20141223",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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