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United States · US · US:41520-507_b1921833-7307-4f20-84bb-d63dab25a76c
CareOne Naproxen Sodium
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAmerican Sales Company
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1141520507711 BOTTLE in 1 CARTON (41520-507-71) / 50 TABLET, FILM COATED in 1 BOTTLE
- ndc1141520507751 BOTTLE in 1 CARTON (41520-507-75) / 90 TABLET, FILM COATED in 1 BOTTLE
- ndc114152050787300 TABLET, FILM COATED in 1 BOTTLE (41520-507-87)
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": {
"206f5483-7de1-4bc3-af27-190e211bcb95": {
"match": "brand_token",
"title": "CAREONE ACID RELIEF (FAMOTIDINE) TABLET, FILM COATED [AMERICAN SALES COMPANY]",
"spl_version": "9",
"published_date": "2026-05-25"
}
},
"productid": "41520-507_b1921833-7307-4f20-84bb-d63dab25a76c",
"productndc": "41520-507",
"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": "CareOne Naproxen Sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA074661",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20160805",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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