Package 82804-206-90

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 82804-206-90
Digits Only 8280420690
Product NDC 82804-206
Product ID 82804-206_64a65366-8577-48f2-9f8e-0332f126d3c1
Description

90 CAPSULE in 1 BOTTLE (82804-206-90)

Marketing

Marketing Status
Marketed Since 2025-03-12
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": "64a65366-8577-48f2-9f8e-0332f126d3c1", "openfda": {"nui": ["N0000008486"], "upc": ["0382804206902"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["64a65366-8577-48f2-9f8e-0332f126d3c1"], "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 (82804-206-90)", "package_ndc": "82804-206-90", "marketing_start_date": "20250312"}], "brand_name": "Gabapentin", "product_id": "82804-206_64a65366-8577-48f2-9f8e-0332f126d3c1", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "82804-206", "generic_name": "Gabapentin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA207099", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}