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United States · US · US:47682-237_3e4cf134-89dd-0093-e063-6394a90a3c63
Medique Mediproxen
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerUnifirst First Aid Corporation
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc114768223733100 PACKET in 1 BOX (47682-237-33) / 1 TABLET, FILM COATED in 1 PACKET (47682-237-46)
- ndc1147682237461 TABLET, FILM COATED in 1 PACKET (47682-237-46)
- ndc11476822375050 PACKET in 1 BOX (47682-237-50) / 1 TABLET, FILM COATED in 1 PACKET
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A079096
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": {
"f01adfcc-b32a-4a98-a4e7-2ce87b824b5a": {
"match": "brand_token",
"title": "MEDIQUE MEDIPROXEN (NAPROXEN SODIUM) TABLET, FILM COATED [SPORTPHARM LLC]",
"spl_version": "2",
"published_date": "2026-04-27"
}
},
"productid": "47682-237_3e4cf134-89dd-0093-e063-6394a90a3c63",
"productndc": "47682-237",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "079096",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Dec 16, 2008"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "Medique Mediproxen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA079096",
"marketing_category": "ANDA",
"nonproprietary_name": "NAPROXEN SODIUM",
"start_marketing_date": "20081230",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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