Package 0904-6665-61
Brand: gabapentin
Generic: gabapentinPackage Facts
Identity
Package NDC
0904-6665-61
Digits Only
0904666561
Product NDC
0904-6665
Description
100 BLISTER PACK in 1 CARTON (0904-6665-61) / 1 CAPSULE 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": "b6880b32-3ebc-4b0e-8a84-d513f3e401af", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430", "310431", "310432"], "spl_set_id": ["36f74fdf-0dae-47a0-a7ea-e64ac91cd88f"], "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 (0904-6665-61) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6665-61", "marketing_start_date": "20110129"}], "brand_name": "Gabapentin", "product_id": "0904-6665_b6880b32-3ebc-4b0e-8a84-d513f3e401af", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "0904-6665", "generic_name": "Gabapentin", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA090858", "marketing_category": "ANDA", "marketing_start_date": "20110129", "listing_expiration_date": "20261231"}