Package 50090-7389-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 50090-7389-0
Digits Only 5009073890
Product NDC 50090-7389
Description

90 CAPSULE in 1 BOTTLE (50090-7389-0)

Marketing

Marketing Status
Marketed Since 2024-10-21
Brand gabapentin
Generic gabapentin
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6ac77dff-8d32-4620-9fbe-08898fdae81f", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["685553b0-384e-400b-a8ae-612ceece8261"], "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 (50090-7389-0)", "package_ndc": "50090-7389-0", "marketing_start_date": "20241021"}], "brand_name": "GABAPENTIN", "product_id": "50090-7389_6ac77dff-8d32-4620-9fbe-08898fdae81f", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7389", "generic_name": "gabapentin", "labeler_name": "A-S Medication Solutions", "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": "20271231"}