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United States · US · US:69842-748_848beb8e-c11f-42b8-8887-cb32ce7659cd
Naproxen Sodium
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCVS Pharmacy
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 7
- ndc11698427480880 CAPSULE, LIQUID FILLED in 1 BOTTLE (69842-748-08)
- ndc116984274816160 CAPSULE, LIQUID FILLED in 1 BOTTLE (69842-748-16)
- ndc1169842748201 BOTTLE, PLASTIC in 1 BOX (69842-748-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
- ndc1169842748301 BOTTLE, PLASTIC in 1 BOX (69842-748-30) / 30 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
- ndc1169842748401 BOTTLE, PLASTIC in 1 BOX (69842-748-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
- ndc1169842748501 BOTTLE, PLASTIC in 1 BOX (69842-748-50) / 50 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
- ndc1169842748801 BOTTLE, PLASTIC in 1 BOX (69842-748-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A208363
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": "69842-748_848beb8e-c11f-42b8-8887-cb32ce7659cd",
"productndc": "69842-748",
"dosage_form": "CAPSULE, LIQUID FILLED",
"orange_book": {
"appl_no": "208363",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 200MG BASE",
"product_no": "001",
"approval_date": "Mar 15, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "Naproxen Sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA208363",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20180401",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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