Package 80425-0163-3

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 80425-0163-3
Digits Only 8042501633
Product NDC 80425-0163
Product ID 80425-0163_2a99b1dd-bed0-79f9-e063-6394a90a35f3
Description

90 CAPSULE in 1 BOTTLE (80425-0163-3)

Marketing

Marketing Status
Marketed Since 2011-01-29
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (1)

Gabapentin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a99b1dd-bed0-79f9-e063-6394a90a35f3", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310432"], "spl_set_id": ["c89a68b6-6dc0-4624-e053-2a95a90a687e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (80425-0163-3)", "package_ndc": "80425-0163-3", "marketing_start_date": "20110129"}], "brand_name": "Gabapentin", "product_id": "80425-0163_2a99b1dd-bed0-79f9-e063-6394a90a35f3", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "80425-0163", "generic_name": "Gabapentin", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "400 mg/1"}], "application_number": "ANDA090858", "marketing_category": "ANDA", "marketing_start_date": "20110129", "listing_expiration_date": "20261231"}