Package 50090-7400-0
Brand: gabapentin
Generic: gabapentinPackage Facts
Identity
Package NDC
50090-7400-0
Digits Only
5009074000
Product NDC
50090-7400
Description
60 TABLET, COATED in 1 BOTTLE (50090-7400-0)
Marketing
Marketing Status
Brand
gabapentin
Generic
gabapentin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7216f0b3-5a46-4015-ac99-6327e840fb69", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["b74a427c-9cc1-4b15-9ed2-cc891741fe67"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (50090-7400-0)", "package_ndc": "50090-7400-0", "marketing_start_date": "20241024"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-7400-1)", "package_ndc": "50090-7400-1", "marketing_start_date": "20241024"}], "brand_name": "Gabapentin", "product_id": "50090-7400_7216f0b3-5a46-4015-ac99-6327e840fb69", "dosage_form": "TABLET, COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7400", "generic_name": "Gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA207057", "marketing_category": "ANDA", "marketing_start_date": "20211101", "listing_expiration_date": "20261231"}