Label: IBUPROFEN AND FAMOTIDINE tablet
- NDC Code(s): 70771-1924-9
- Packager: Zydus Lifesciences Limited
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated May 28, 2025
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PACKAGE LABEL.PRINCIPAL DISPLAY PANELIbuprofen and famotidine tablets, 800 mg/26.6 mg - 90 Tablets - NDC 70771-1924-9 - Rx only
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INGREDIENTS AND APPEARANCEProduct Information