Package 0904-6823-61
Brand: gabapentin
Generic: gabapentinPackage Facts
Identity
Package NDC
0904-6823-61
Digits Only
0904682361
Product NDC
0904-6823
Description
100 BLISTER PACK in 1 CARTON (0904-6823-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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": "3e587d00-7f5f-42dc-b941-9796ee032327", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["152adf1d-ec0c-4561-bf80-e4c7da158723"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6823-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6823-61", "marketing_start_date": "20111006"}], "brand_name": "Gabapentin", "product_id": "0904-6823_3e587d00-7f5f-42dc-b941-9796ee032327", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "0904-6823", "generic_name": "Gabapentin", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA200651", "marketing_category": "ANDA", "marketing_start_date": "20111006", "listing_expiration_date": "20261231"}