Package 0641-0476-25

Brand: phenobarbital sodium

Generic: phenobarbital sodium
NDC Package

Package Facts

Identity

Package NDC 0641-0476-25
Digits Only 0641047625
Product NDC 0641-0476
Product ID 0641-0476_57a9cc7f-aead-4434-942f-363a419ea385
Description

25 VIAL in 1 CARTON (0641-0476-25) / 1 mL in 1 VIAL (0641-0476-21)

Marketing

Marketing Status
Marketed Since 1971-01-01
Brand phenobarbital sodium
Generic phenobarbital sodium
Sample Package No

Linked Drug Pages (1)

Phenobarbital Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "57a9cc7f-aead-4434-942f-363a419ea385", "openfda": {"upc": ["0306410477259"], "unii": ["SW9M9BB5K3"], "rxcui": ["198368", "312370"], "spl_set_id": ["ffcaa218-ed6a-4557-9645-b9a91128a214"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0641-0476-25)  / 1 mL in 1 VIAL (0641-0476-21)", "package_ndc": "0641-0476-25", "marketing_start_date": "19710101"}], "brand_name": "Phenobarbital Sodium", "product_id": "0641-0476_57a9cc7f-aead-4434-942f-363a419ea385", "dosage_form": "INJECTION", "product_ndc": "0641-0476", "dea_schedule": "CIV", "generic_name": "Phenobarbital Sodium", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital Sodium", "active_ingredients": [{"name": "PHENOBARBITAL SODIUM", "strength": "65 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19710101", "listing_expiration_date": "20261231"}