Package 42806-657-09

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 42806-657-09
Digits Only 4280665709
Product NDC 42806-657
Product ID 42806-657_c48c3c6d-4407-4312-8e81-46db64698cb7
Description

90 TABLET in 1 BOTTLE (42806-657-09)

Marketing

Marketing Status
Marketed Since 2024-02-26
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": "c48c3c6d-4407-4312-8e81-46db64698cb7", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["1806380", "1806382"], "spl_set_id": ["d592d828-8df1-480d-b179-bb9260a9c824"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (42806-657-09)", "package_ndc": "42806-657-09", "marketing_start_date": "20240226"}], "brand_name": "Gabapentin", "product_id": "42806-657_c48c3c6d-4407-4312-8e81-46db64698cb7", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "42806-657", "generic_name": "Gabapentin", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA216252", "marketing_category": "ANDA", "marketing_start_date": "20240226", "listing_expiration_date": "20261231"}