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United States · US · US:27854-165_6cbf25c7-2930-4fa4-84fa-01fe19cf6299
Flanax Menstrual Pain Reliever
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 · 1
- ndc1127854165101 BOTTLE, PLASTIC in 1 CARTON (27854-165-10) / 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A204872
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": "27854-165_6cbf25c7-2930-4fa4-84fa-01fe19cf6299",
"productndc": "27854-165",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "204872",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Jan 23, 2017"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "Flanax Menstrual Pain Reliever",
"active_ingred_unit": "mg/1",
"application_number": "ANDA204872",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20170123",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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