Package 71610-426-60

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 71610-426-60
Digits Only 7161042660
Product NDC 71610-426
Description

90 TABLET, FILM COATED in 1 BOTTLE (71610-426-60)

Marketing

Marketing Status
Marketed Since 2020-05-15
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": "f44af22b-a99e-4c28-94af-f260bbb6ba0f", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["ba2a8352-5776-4edb-914e-ce1d18ccda32"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-426-60)", "package_ndc": "71610-426-60", "marketing_start_date": "20200515"}], "brand_name": "Gabapentin", "product_id": "71610-426_f44af22b-a99e-4c28-94af-f260bbb6ba0f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71610-426", "generic_name": "GABAPENTIN", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA203244", "marketing_category": "ANDA", "marketing_start_date": "20140111", "listing_expiration_date": "20261231"}