Package 51672-4005-3
Brand: carbamazepine
Generic: carbamazepinePackage Facts
Identity
Package NDC
51672-4005-3
Digits Only
5167240053
Product NDC
51672-4005
Description
1000 TABLET in 1 BOTTLE (51672-4005-3)
Marketing
Marketing Status
Brand
carbamazepine
Generic
carbamazepine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48fd19fc-5d5b-0d24-e063-6294a90a0aa0", "openfda": {"nui": ["N0000008486", "N0000175751", "N0000185506", "N0000191266", "N0000187064", "N0000185507", "N0000185607"], "upc": ["0351672405014", "0351672412418", "0351672404741"], "unii": ["33CM23913M"], "rxcui": ["197442", "199378", "308973", "308976", "308979", "402505", "402506"], "spl_set_id": ["0526a054-3eda-49b4-b390-7d5d16e30af8"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Mood Stabilizer [EPC]"], "pharm_class_moa": ["Cytochrome P450 3A4 Inducers [MoA]", "Cytochrome P450 1A2 Inducers [MoA]", "Cytochrome P450 2B6 Inducers [MoA]", "Cytochrome P450 2C9 Inducers [MoA]", "Cytochrome P450 2C19 Inducers [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (51672-4005-1)", "package_ndc": "51672-4005-1", "marketing_start_date": "19961003"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (51672-4005-2)", "package_ndc": "51672-4005-2", "marketing_start_date": "19961003"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (51672-4005-3)", "package_ndc": "51672-4005-3", "marketing_start_date": "19961003"}], "brand_name": "Carbamazepine", "product_id": "51672-4005_48fd19fc-5d5b-0d24-e063-6294a90a0aa0", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inducers [MoA]", "Cytochrome P450 2B6 Inducers [MoA]", "Cytochrome P450 2C19 Inducers [MoA]", "Cytochrome P450 2C9 Inducers [MoA]", "Cytochrome P450 3A4 Inducers [MoA]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "51672-4005", "generic_name": "Carbamazepine", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carbamazepine", "active_ingredients": [{"name": "CARBAMAZEPINE", "strength": "200 mg/1"}], "application_number": "ANDA074649", "marketing_category": "ANDA", "marketing_start_date": "19961003", "listing_expiration_date": "20271231"}