Package 67296-2192-3

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 67296-2192-3
Digits Only 6729621923
Product NDC 67296-2192
Product ID 67296-2192_44f2bb79-7a83-d8ee-e063-6394a90aa874
Description

30 CAPSULE in 1 BOTTLE (67296-2192-3)

Marketing

Marketing Status
Marketed Since 2021-05-10
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": "44f2bb79-7a83-d8ee-e063-6394a90aa874", "openfda": {"nui": ["N0000008486"], "upc": ["0331722148054"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["44f2b497-55b2-864f-e063-6294a90ad6d5"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (67296-2192-3)", "package_ndc": "67296-2192-3", "marketing_start_date": "20210510"}], "brand_name": "GABAPENTIN", "product_id": "67296-2192_44f2bb79-7a83-d8ee-e063-6394a90aa874", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "67296-2192", "generic_name": "gabapentin", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA214956", "marketing_category": "ANDA", "marketing_start_date": "20210510", "listing_expiration_date": "20261231"}