Package 82619-145-01

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 82619-145-01
Digits Only 8261914501
Product NDC 82619-145
Description

100 TABLET in 1 BOTTLE (82619-145-01)

Marketing

Marketing Status
Marketed Since 2024-09-01
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": "26ce27e6-34a6-70d2-e063-6394a90a7c96", "openfda": {"nui": ["N0000008486"], "upc": ["0382619142020", "0382619143034", "0382619143027", "0382619144017", "0382619146011", "0382619144024", "0382619142013", "0382619143010", "0382619145014", "0382619142037", "0382619146028", "0382619145021"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["266ef369-0a56-f225-e063-6294a90a495e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Creekwood Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82619-145-01)", "package_ndc": "82619-145-01", "marketing_start_date": "20240901"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82619-145-02)", "package_ndc": "82619-145-02", "marketing_start_date": "20240901"}], "brand_name": "Gabapentin", "product_id": "82619-145_26ce27e6-34a6-70d2-e063-6394a90a7c96", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "82619-145", "generic_name": "Gabapentin", "labeler_name": "Creekwood Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA205101", "marketing_category": "ANDA", "marketing_start_date": "20240901", "listing_expiration_date": "20261231"}