{
"NDC": {
"NDCCode": "75907-432-01",
"PackageDescription": "1 BOTTLE in 1 CARTON (75907-432-01) / 100 TABLET in 1 BOTTLE",
"NDC11Code": "75907-0432-01",
"ProductNDC": "75907-432",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Acetaminophen Aspirin Caffeine",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Acetaminophen Aspirin Caffeine",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20260925",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA214039",
"LabelerName": "Dr. Reddy's Laboratories Inc.",
"SubstanceName": "ACETAMINOPHEN; CAFFEINE; ASPIRIN",
"StrengthNumber": "250; 65; 250",
"StrengthUnit": "mg/1; mg/1; mg/1",
"Pharm_Classes": "Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-09-26",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260925",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}