Package 68788-8641-6

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 68788-8641-6
Digits Only 6878886416
Product NDC 68788-8641
Description

60 TABLET, FILM COATED in 1 BOTTLE (68788-8641-6)

Marketing

Marketing Status
Marketed Since 2024-04-29
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": "4e11eb11-0799-4f14-8e8f-659a85df1739", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["8b1aa8bf-db72-460a-98de-cd8180608f01"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-8641-1)", "package_ndc": "68788-8641-1", "marketing_start_date": "20240429"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8641-3)", "package_ndc": "68788-8641-3", "marketing_start_date": "20240429"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8641-6)", "package_ndc": "68788-8641-6", "marketing_start_date": "20240429"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68788-8641-8)", "package_ndc": "68788-8641-8", "marketing_start_date": "20240429"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8641-9)", "package_ndc": "68788-8641-9", "marketing_start_date": "20240429"}], "brand_name": "Gabapentin", "product_id": "68788-8641_4e11eb11-0799-4f14-8e8f-659a85df1739", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68788-8641", "generic_name": "GABAPENTIN", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA203244", "marketing_category": "ANDA", "marketing_start_date": "20240429", "listing_expiration_date": "20261231"}