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United States · US · US:11673-368_25a249be-b52a-4d7e-8352-8e6d30f3664f
up and up naproxen sodium
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTarget Corporation
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1111673368711 BOTTLE in 1 CARTON (11673-368-71) / 50 TABLET, FILM COATED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A074661
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": {
"51c0a953-93cb-4d0a-b51c-02d9482d1746": {
"match": "brand_token",
"title": "UP AND UP ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [TARGET CORPORATION]",
"spl_version": "12",
"published_date": "2026-05-13"
}
},
"productid": "11673-368_25a249be-b52a-4d7e-8352-8e6d30f3664f",
"productndc": "11673-368",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "074661",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Jan 13, 1997"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "up and up naproxen sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA074661",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20090624",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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