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United States · US · US:27854-700_4215c852-11ed-4b06-b132-3674265078e3
Flanax Pain Reliever/Fever Reducer
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBelmora LLC
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1127854700011 BOTTLE in 1 CARTON (27854-700-01) / 24 TABLET, FILM COATED in 1 BOTTLE
- ndc1127854700101 BOTTLE in 1 CARTON (27854-700-10) / 10 TABLET, FILM COATED in 1 BOTTLE
- ndc1127854700991 BOTTLE in 1 CARTON (27854-700-99) / 100 TABLET, FILM COATED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A205497
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": {
"2b4135b3-389c-46e2-ae86-7674c2ab9a32": {
"match": "brand_token",
"title": "FLANAX MENSTRUAL PAIN RELIEVER (NAPROXEN SODIUM) TABLET, FILM COATED [BELMORA LLC]",
"spl_version": "15",
"published_date": "2026-01-28"
}
},
"productid": "27854-700_4215c852-11ed-4b06-b132-3674265078e3",
"productndc": "27854-700",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "205497",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Mar 18, 2016"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "Flanax Pain Reliever/Fever Reducer",
"active_ingred_unit": "mg/1",
"application_number": "ANDA205497",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen sodium",
"start_marketing_date": "20200515",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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