Package 50090-7673-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 50090-7673-0
Digits Only 5009076730
Product NDC 50090-7673
Description

90 CAPSULE in 1 BOTTLE (50090-7673-0)

Marketing

Marketing Status
Marketed Since 2025-10-08
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": "01196905-4565-450b-8c37-8ed986ed3adb", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["1ead7343-ab25-41b5-af4f-f903470e1dd9"], "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 (50090-7673-0)", "package_ndc": "50090-7673-0", "marketing_start_date": "20251008"}], "brand_name": "Gabapentin", "product_id": "50090-7673_01196905-4565-450b-8c37-8ed986ed3adb", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7673", "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": "ANDA204989", "marketing_category": "ANDA", "marketing_start_date": "20160218", "listing_expiration_date": "20261231"}