Package 50090-7715-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 50090-7715-0
Digits Only 5009077150
Product NDC 50090-7715
Description

90 TABLET in 1 BOTTLE (50090-7715-0)

Marketing

Marketing Status
Marketed Since 2025-10-15
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": "dc6a24e2-c58b-44d2-9491-3538d0e507fd", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["aa246838-609c-4254-a8ec-d6f463a17960"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7715-0)", "package_ndc": "50090-7715-0", "marketing_start_date": "20251015"}], "brand_name": "Gabapentin", "product_id": "50090-7715_dc6a24e2-c58b-44d2-9491-3538d0e507fd", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7715", "generic_name": "Gabapentin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA217995", "marketing_category": "ANDA", "marketing_start_date": "20240404", "listing_expiration_date": "20261231"}