Package 82804-178-90

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 82804-178-90
Digits Only 8280417890
Product NDC 82804-178
Product ID 82804-178_481e6b68-50e4-4594-9815-32580a84ab8c
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (82804-178-90)

Marketing

Marketing Status
Marketed Since 2024-12-16
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": "481e6b68-50e4-4594-9815-32580a84ab8c", "openfda": {"nui": ["N0000008486"], "upc": ["0382804178902"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["481e6b68-50e4-4594-9815-32580a84ab8c"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (82804-178-90)", "package_ndc": "82804-178-90", "marketing_start_date": "20241216"}], "brand_name": "Gabapentin", "product_id": "82804-178_481e6b68-50e4-4594-9815-32580a84ab8c", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "82804-178", "generic_name": "Gabapentin", "labeler_name": "Proficient Rx LP", "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"}