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United States · US · US:49035-382_f0fb53cd-5c61-6417-e053-2995a90a6c61
Naproxen Sodium
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWal-Mart Stores, Inc.
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc114903538222120 CAPSULE, LIQUID FILLED in 1 BOTTLE (49035-382-22)
- ndc11490353827880 CAPSULE, LIQUID FILLED in 1 BOTTLE (49035-382-78)
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
N021920
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": "49035-382_f0fb53cd-5c61-6417-e053-2995a90a6c61",
"productndc": "49035-382",
"dosage_form": "CAPSULE, LIQUID FILLED",
"orange_book": {
"appl_no": "021920",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "EQ 200MG BASE",
"product_no": "001",
"approval_date": "Feb 17, 2006"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "Naproxen Sodium",
"active_ingred_unit": "mg/1",
"application_number": "NDA021920",
"marketing_category": "NDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20200301",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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