Package 61919-640-30

Brand: gabapentin

Generic: gabapentin
NDC Package

Package Facts

Identity

Package NDC 61919-640-30
Digits Only 6191964030
Product NDC 61919-640
Product ID 61919-640_47e158f3-f67b-74b2-e063-6394a90ac498
Description

30 CAPSULE in 1 BOTTLE (61919-640-30)

Marketing

Marketing Status
Marketed Since 2019-04-09
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": "47e158f3-f67b-74b2-e063-6394a90ac498", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310431"], "spl_set_id": ["29a70e2d-d3fd-4e32-95dd-7ee721d87388"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (61919-640-30)", "package_ndc": "61919-640-30", "marketing_start_date": "20190409"}], "brand_name": "GABAPENTIN", "product_id": "61919-640_47e158f3-f67b-74b2-e063-6394a90ac498", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "61919-640", "generic_name": "GABAPENTIN", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "300 mg/1"}], "application_number": "ANDA090007", "marketing_category": "ANDA", "marketing_start_date": "20151230", "listing_expiration_date": "20271231"}