Package 70518-1834-0

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 70518-1834-0
Digits Only 7051818340
Product NDC 70518-1834
Product ID 70518-1834_49770231-ffd0-bb75-e063-6394a90aa7fb
Description

30 CAPSULE in 1 BLISTER PACK (70518-1834-0)

Marketing

Marketing Status
Marketed Since 2019-01-30
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": "49770231-ffd0-bb75-e063-6394a90aa7fb", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310430"], "spl_set_id": ["7652adc6-1aad-4422-b85c-0c6b11c23b73"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-1834-0)", "package_ndc": "70518-1834-0", "marketing_start_date": "20190130"}], "brand_name": "Gabapentin", "product_id": "70518-1834_49770231-ffd0-bb75-e063-6394a90aa7fb", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-1834", "generic_name": "Gabapentin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "100 mg/1"}], "application_number": "ANDA090858", "marketing_category": "ANDA", "marketing_start_date": "20190130", "listing_expiration_date": "20271231"}