Package 16571-675-16

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 16571-675-16
Digits Only 1657167516
Product NDC 16571-675
Product ID 16571-675_a84eee2c-e36f-478c-8793-b153799ea38b
Description

473 mL in 1 BOTTLE (16571-675-16)

Marketing

Marketing Status
Marketed Since 2020-09-01
Brand phenobarbital
Generic phenobarbital
Sample Package No

Linked Drug Pages (1)

Phenobarbital ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a84eee2c-e36f-478c-8793-b153799ea38b", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["702519"], "spl_set_id": ["fe874f8a-4b56-4d2b-abf5-8742e2633a3b"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (16571-675-16)", "package_ndc": "16571-675-16", "marketing_start_date": "20200901"}], "brand_name": "Phenobarbital", "product_id": "16571-675_a84eee2c-e36f-478c-8793-b153799ea38b", "dosage_form": "LIQUID", "product_ndc": "16571-675", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "20 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20200901", "listing_expiration_date": "20261231"}