Package 70771-1842-1
Brand: oxcarbazepine
Generic: oxcarbazepinePackage Facts
Identity
Package NDC
70771-1842-1
Digits Only
7077118421
Product NDC
70771-1842
Description
100 TABLET in 1 BOTTLE (70771-1842-1)
Marketing
Marketing Status
Brand
oxcarbazepine
Generic
oxcarbazepine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "905fd0b0-fd53-48f5-83ff-129a5f5f104c", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0370771184415", "0370771184217", "0370771184316"], "unii": ["VZI5B1W380"], "rxcui": ["312136", "312137", "312138"], "spl_set_id": ["e23d8a74-b47b-462a-b09c-90bdd58a032e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1842-1)", "package_ndc": "70771-1842-1", "marketing_start_date": "20250710"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1842-4) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "70771-1842-4", "marketing_start_date": "20250710"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70771-1842-5)", "package_ndc": "70771-1842-5", "marketing_start_date": "20250710"}], "brand_name": "oxcarbazepine", "product_id": "70771-1842_905fd0b0-fd53-48f5-83ff-129a5f5f104c", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70771-1842", "generic_name": "oxcarbazepine", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "oxcarbazepine", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "150 mg/1"}], "application_number": "ANDA211747", "marketing_category": "ANDA", "marketing_start_date": "20250710", "listing_expiration_date": "20261231"}