Package 81033-164-47

Brand: phenobarbital oral solution

Generic: phenobarbital oral
NDC Package

Package Facts

Identity

Package NDC 81033-164-47
Digits Only 8103316447
Product NDC 81033-164
Description

473 mL in 1 BOTTLE, PLASTIC (81033-164-47)

Marketing

Marketing Status
Marketed Since 2025-11-05
Brand phenobarbital oral solution
Generic phenobarbital oral
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "446d8928-62fe-1d8e-e063-6394a90a2fe2", "openfda": {"upc": ["0381033164472"], "unii": ["YQE403BP4D"], "rxcui": ["702519"], "spl_set_id": ["446d88cb-31bd-5aa5-e063-6294a90a8dc0"], "manufacturer_name": ["Kesin Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (81033-164-47)", "package_ndc": "81033-164-47", "marketing_start_date": "20251105"}], "brand_name": "Phenobarbital Oral Solution", "product_id": "81033-164_446d8928-62fe-1d8e-e063-6394a90a2fe2", "dosage_form": "SOLUTION", "product_ndc": "81033-164", "dea_schedule": "CIV", "generic_name": "Phenobarbital Oral", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital Oral Solution", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "20 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20251105", "listing_expiration_date": "20261231"}