Package 16714-332-01

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 16714-332-01
Digits Only 1671433201
Product NDC 16714-332
Product ID 16714-332_e1bc9060-641c-4196-acfd-676a3d263fed
Description

100 TABLET, FILM COATED in 1 BOTTLE (16714-332-01)

Marketing

Marketing Status
Marketed Since 2011-10-06
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": "e1bc9060-641c-4196-acfd-676a3d263fed", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["9508cb1b-3f9f-48bd-8f34-a6fbb68c9a4a"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16714-332-01)", "package_ndc": "16714-332-01", "marketing_start_date": "20111006"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (16714-332-02)", "package_ndc": "16714-332-02", "marketing_start_date": "20111006"}], "brand_name": "Gabapentin", "product_id": "16714-332_e1bc9060-641c-4196-acfd-676a3d263fed", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "16714-332", "generic_name": "Gabapentin", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA200651", "marketing_category": "ANDA", "marketing_start_date": "20111006", "listing_expiration_date": "20261231"}