Package 50268-326-13

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 50268-326-13
Digits Only 5026832613
Product NDC 50268-326
Product ID 50268-326_2b48eef3-a050-7828-e063-6294a90a4a83
Description

30 BLISTER PACK in 1 BOX (50268-326-13) / 1 TABLET, COATED in 1 BLISTER PACK (50268-326-11)

Marketing

Marketing Status
Marketed Since 2023-08-08
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": "2b48eef3-a050-7828-e063-6294a90a4a83", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["026a7219-78ba-48c7-e063-6394a90ad736"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX (50268-326-13)  / 1 TABLET, COATED in 1 BLISTER PACK (50268-326-11)", "package_ndc": "50268-326-13", "marketing_start_date": "20230808"}], "brand_name": "Gabapentin", "product_id": "50268-326_2b48eef3-a050-7828-e063-6294a90a4a83", "dosage_form": "TABLET, COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50268-326", "generic_name": "Gabapentin", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA207057", "marketing_category": "ANDA", "marketing_start_date": "20230808", "listing_expiration_date": "20261231"}