Package 82804-210-90

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 82804-210-90
Digits Only 8280421090
Product NDC 82804-210
Description

90 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-210-90)

Marketing

Marketing Status
Marketed Since 2025-03-01
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": "0ad67a07-59d0-4aaa-906b-befbbad8af31", "openfda": {"nui": ["N0000008486"], "upc": ["0382804210909"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["0ad67a07-59d0-4aaa-906b-befbbad8af31"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (82804-210-90)", "package_ndc": "82804-210-90", "marketing_start_date": "20250301"}], "brand_name": "Gabapentin", "product_id": "82804-210_0ad67a07-59d0-4aaa-906b-befbbad8af31", "dosage_form": "TABLET, COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "82804-210", "generic_name": "Gabapentin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA207057", "marketing_category": "ANDA", "marketing_start_date": "20211101", "listing_expiration_date": "20261231"}