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United States · US · US:80267-001_eaf6d2fc-ebcb-4d11-8e3f-a494f0f7920b
betr headache pain relief
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLive Betr LLC
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1180267001711 BOTTLE in 1 CARTON (80267-001-71) / 50 TABLET, FILM COATED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A074661
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": {
"8c2d5514-62c1-4e98-8412-20534365b934": {
"match": "brand_token",
"title": "BETR SLEEP AID (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [LIVE BETR LLC]",
"spl_version": "4",
"published_date": "2024-07-24"
}
},
"productid": "80267-001_eaf6d2fc-ebcb-4d11-8e3f-a494f0f7920b",
"productndc": "80267-001",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "074661",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Jan 13, 1997"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "betr headache pain relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA074661",
"marketing_category": "ANDA",
"nonproprietary_name": "naproxen sodium",
"start_marketing_date": "20210209",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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