Package 72162-1534-1

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 72162-1534-1
Digits Only 7216215341
Product NDC 72162-1534
Product ID 72162-1534_85994fa2-027d-4563-846e-a1c86c966e82
Description

100 CAPSULE in 1 BOTTLE, PLASTIC (72162-1534-1)

Marketing

Marketing Status
Marketed Since 2024-02-02
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": "85994fa2-027d-4563-846e-a1c86c966e82", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310432"], "spl_set_id": ["43cbff48-8219-41ba-b67d-3ae4544b78bb"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (72162-1534-1)", "package_ndc": "72162-1534-1", "marketing_start_date": "20240202"}], "brand_name": "Gabapentin", "product_id": "72162-1534_85994fa2-027d-4563-846e-a1c86c966e82", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72162-1534", "generic_name": "Gabapentin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "400 mg/1"}], "application_number": "ANDA204989", "marketing_category": "ANDA", "marketing_start_date": "20160218", "listing_expiration_date": "20261231"}