Package 68071-2214-9

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 68071-2214-9
Digits Only 6807122149
Product NDC 68071-2214
Product ID 68071-2214_1d7609b9-edf7-178d-e063-6294a90a3626
Description

90 TABLET in 1 BOTTLE (68071-2214-9)

Marketing

Marketing Status
Marketed Since 2020-07-08
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": "1d7609b9-edf7-178d-e063-6294a90a3626", "openfda": {"nui": ["N0000008486"], "upc": ["0368071221497"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["a9f0852e-0c58-ba22-e053-2995a90adfa0"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-2214-9)", "package_ndc": "68071-2214-9", "marketing_start_date": "20200708"}], "brand_name": "Gabapentin", "product_id": "68071-2214_1d7609b9-edf7-178d-e063-6294a90a3626", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68071-2214", "generic_name": "Gabapentin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA205101", "marketing_category": "ANDA", "marketing_start_date": "20160204", "listing_expiration_date": "20261231"}