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United States · US · US:48201-007_4240708f-eaa2-9c13-e063-6294a90ab632
CALMADOL PAIN RELIEVER
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGRANDALL DISTRIBUTING, LLC
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1148201007241 PACKET in 1 BOX (48201-007-24) / 24 TABLET in 1 PACKET
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A090545
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": {
"31b7f84e-8b66-4d31-8e9c-279d0af2fe64": {
"match": "brand_token",
"title": "CALMADOL (CAMPHOR, MENTHOL, METHYL SALICYLATE) LINIMENT [GRANDALL DISTRIBUTING, LLC]",
"spl_version": "11",
"published_date": "2025-11-17"
}
},
"productid": "48201-007_4240708f-eaa2-9c13-e063-6294a90ab632",
"productndc": "48201-007",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "090545",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Mar 16, 2011"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "CALMADOL PAIN RELIEVER",
"active_ingred_unit": "mg/1",
"application_number": "ANDA090545",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20150331",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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