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United States · US · US:0363-0177_da638473-feb5-ccf1-e053-2a95a90a80d3
Naproxen Sodium
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWALGREEN COMPANY
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 7
- ndc1103630177111 BOTTLE, PLASTIC in 1 CARTON (0363-0177-11) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
- ndc1103630177151 BOTTLE, PLASTIC in 1 CARTON (0363-0177-15) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
- ndc1103630177161 BOTTLE, PLASTIC in 1 CARTON (0363-0177-16) / 50 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
- ndc1103630177221 BOTTLE, PLASTIC in 1 CARTON (0363-0177-22) / 120 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
- ndc110363017725180 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0363-0177-25)
- ndc1103630177781 BOTTLE, PLASTIC in 1 CARTON (0363-0177-78) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
- ndc11036301779980 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0363-0177-99)
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": "0363-0177_da638473-feb5-ccf1-e053-2a95a90a80d3",
"productndc": "0363-0177",
"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": "20190802",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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