Package 51224-021-60

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 51224-021-60
Digits Only 5122402160
Product NDC 51224-021
Description

500 TABLET, COATED in 1 BOTTLE (51224-021-60)

Marketing

Marketing Status
Marketed Since 2019-05-01
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": "001831ce-47e9-4d0e-9aa5-d566575c2267", "openfda": {"nui": ["N0000008486"], "upc": ["0351224121508", "0351224021501"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["725878fa-1e2f-4fee-a9e1-a6e102c79625"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["TAGI Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (51224-021-60)", "package_ndc": "51224-021-60", "marketing_start_date": "20190501"}], "brand_name": "Gabapentin", "product_id": "51224-021_001831ce-47e9-4d0e-9aa5-d566575c2267", "dosage_form": "TABLET, COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "51224-021", "generic_name": "Gabapentin", "labeler_name": "TAGI Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA207057", "marketing_category": "ANDA", "marketing_start_date": "20190501", "listing_expiration_date": "20271231"}