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United States · US · US:56062-194_106cff2c-1d3b-4f5d-ab79-5f67e04594d6
maximum strength
Orange BookUNIISPLATC A02BA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPublix Super Markets Inc
CountryUS (United States)
ATC codeA02BA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11560621940225 BLISTER PACK in 1 CARTON (56062-194-02) / 1 TABLET, FILM COATED in 1 BLISTER PACK
- ndc1156062194711 BOTTLE in 1 CARTON (56062-194-71) / 50 TABLET, FILM COATED in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
5QZO15J2Z8
FAMOTIDINE
RxCUI 4278
Orange Book
A077351
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "5QZO15J2Z8",
"rxcui": "4278",
"inchikey": "XUFQPHANEAPEMJ-UHFFFAOYSA-N",
"display_name": "FAMOTIDINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"350764de-7801-b24e-e063-6394a90ab3c3": {
"match": "brand_token",
"title": "MAXIMUM STRENGTH MUCINEX SINUS-MAX PRESSURE, PAIN AND COUGH (ACETAMINOPHEN, GUAIFENESIN) TABLET, FILM COATED [RECKITT BENCKISER LLC]",
"spl_version": "2",
"published_date": "2026-05-15"
}
},
"productid": "56062-194_106cff2c-1d3b-4f5d-ab79-5f67e04594d6",
"productndc": "56062-194",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "077351",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "20MG",
"product_no": "001",
"approval_date": "Sep 25, 2006"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "FAMOTIDINE",
"proprietary_name": "maximum strength",
"active_ingred_unit": "mg/1",
"application_number": "ANDA077351",
"marketing_category": "ANDA",
"nonproprietary_name": "Famotidine",
"start_marketing_date": "20071203",
"active_numerator_strength": "20"
}Related drugs
Other records sharing ATC code A02BA03.
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