Package 68071-3783-9
Brand: gabapentin
Generic: gabapentinPackage Facts
Identity
Package NDC
68071-3783-9
Digits Only
6807137839
Product NDC
68071-3783
Description
90 TABLET, COATED in 1 BOTTLE, PLASTIC (68071-3783-9)
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": "2c65033f-5eb1-27df-e063-6394a90a8c0c", "openfda": {"nui": ["N0000008486"], "upc": ["0368071378399"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["2c65253d-ca49-70eb-e063-6394a90a3cd2"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (68071-3783-9)", "package_ndc": "68071-3783-9", "marketing_start_date": "20250123"}], "brand_name": "Gabapentin", "product_id": "68071-3783_2c65033f-5eb1-27df-e063-6394a90a8c0c", "dosage_form": "TABLET, COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68071-3783", "generic_name": "Gabapentin", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA207057", "marketing_category": "ANDA", "marketing_start_date": "20211101", "listing_expiration_date": "20261231"}