Package 0904-6575-80

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 0904-6575-80
Digits Only 0904657580
Product NDC 0904-6575
Description

1000 TABLET in 1 BOTTLE, PLASTIC (0904-6575-80)

Marketing

Marketing Status
Discontinued 2026-05-31
Brand phenobarbital
Generic phenobarbital
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fae5ad4d-d64e-4517-9bea-eac6d833bd5d", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["199167"], "spl_set_id": ["e024b80b-c22f-44bc-b273-f9398f840ed0"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6575-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6575-61", "marketing_start_date": "20030201"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0904-6575-80)", "package_ndc": "0904-6575-80", "marketing_end_date": "20260531", "marketing_start_date": "20030201"}], "brand_name": "Phenobarbital", "product_id": "0904-6575_fae5ad4d-d64e-4517-9bea-eac6d833bd5d", "dosage_form": "TABLET", "product_ndc": "0904-6575", "dea_schedule": "CIV", "generic_name": "phenobarbital", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "32.4 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20030201", "listing_expiration_date": "20261231"}