Package 50268-325-15

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 50268-325-15
Digits Only 5026832515
Product NDC 50268-325
Description

50 BLISTER PACK in 1 BOX (50268-325-15) / 1 TABLET, COATED in 1 BLISTER PACK (50268-325-11)

Marketing

Marketing Status
Marketed Since 2023-05-01
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": "2b4c1c97-dc71-3801-e063-6394a90a7faf", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["faa47fcd-2545-a946-e053-6294a90a05d2"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-325-15)  / 1 TABLET, COATED in 1 BLISTER PACK (50268-325-11)", "package_ndc": "50268-325-15", "marketing_start_date": "20230501"}], "brand_name": "Gabapentin", "product_id": "50268-325_2b4c1c97-dc71-3801-e063-6394a90a7faf", "dosage_form": "TABLET, COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50268-325", "generic_name": "Gabapentin", "labeler_name": "AvPAK", "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": "20230501", "listing_expiration_date": "20261231"}