phenobarbital

Generic: phenobarbital

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenobarbital
Generic Name phenobarbital
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenobarbital 32.4 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6575
Product ID 0904-6575_fae5ad4d-d64e-4517-9bea-eac6d833bd5d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2003-02-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046575
Hyphenated Format 0904-6575

Supplemental Identifiers

RxCUI
199167
UNII
YQE403BP4D

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name phenobarbital (source: ndc)
Generic Name phenobarbital (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 32.4 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-6575-61) / 1 TABLET in 1 BLISTER PACK
  • 1000 TABLET in 1 BOTTLE, PLASTIC (0904-6575-80)
source: ndc

Packages (2)

0904-6575-61 100 BLISTER PACK in 1 CARTON (0904-6575-61) / 1 TABLET in 1 BLISTER PACK 0904-6575-80 1000 TABLET in 1 BOTTLE, PLASTIC (0904-6575-80)

Ingredients (1)

phenobarbital (32.4 mg/1)

Linked Drug Pages (1)

Phenobarbital ndc-match (0.9)

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"}