Package 68001-412-00

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 68001-412-00
Digits Only 6800141200
Product NDC 68001-412
Description

100 TABLET in 1 BOTTLE (68001-412-00)

Marketing

Marketing Status
Marketed Since 2019-09-30
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": "3e4d1b97-0022-6671-e063-6294a90ae02d", "openfda": {"nui": ["N0000008486"], "upc": ["0368001412001", "0368001411004"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["3368bf70-d466-4765-b2b7-7fe967a8c2b7"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68001-412-00)", "package_ndc": "68001-412-00", "marketing_start_date": "20190930"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68001-412-03)", "package_ndc": "68001-412-03", "marketing_start_date": "20190930"}], "brand_name": "Gabapentin", "product_id": "68001-412_3e4d1b97-0022-6671-e063-6294a90ae02d", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68001-412", "generic_name": "Gabapentin", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA077662", "marketing_category": "ANDA", "marketing_start_date": "20190930", "listing_expiration_date": "20261231"}