Package 50090-7421-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 50090-7421-0
Digits Only 5009074210
Product NDC 50090-7421
Product ID 50090-7421_514712a8-b6ce-4d2f-9c3a-0f4f37b7ba7c
Description

90 CAPSULE in 1 BOTTLE (50090-7421-0)

Marketing

Marketing Status
Marketed Since 2024-10-28
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": "514712a8-b6ce-4d2f-9c3a-0f4f37b7ba7c", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["4aa69d04-6b32-4764-a48b-ef5313dd95d3"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-7421-0)", "package_ndc": "50090-7421-0", "marketing_start_date": "20241028"}], "brand_name": "GABAPENTIN", "product_id": "50090-7421_514712a8-b6ce-4d2f-9c3a-0f4f37b7ba7c", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7421", "generic_name": "gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA214956", "marketing_category": "ANDA", "marketing_start_date": "20210510", "listing_expiration_date": "20271231"}