phenobarbital

Generic: phenobarbital

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenobarbital
Generic Name phenobarbital
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenobarbital 64.8 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-984
Product ID 82804-984_6b5ca781-50a9-4e89-8184-831c7c2936b2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2023-09-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804984
Hyphenated Format 82804-984

Supplemental Identifiers

RxCUI
198086 199164 199167 199168
UPC
0382804984305 0382804982301 0382804983308 0382804985302
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
  • 64.8 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (82804-984-00)
  • 1000 TABLET in 1 BOTTLE (82804-984-11)
  • 30 TABLET in 1 BOTTLE (82804-984-30)
  • 500 TABLET in 1 BOTTLE (82804-984-55)
  • 60 TABLET in 1 BOTTLE (82804-984-60)
  • 90 TABLET in 1 BOTTLE (82804-984-90)
source: ndc

Packages (6)

82804-984-00 100 TABLET in 1 BOTTLE (82804-984-00) 82804-984-11 1000 TABLET in 1 BOTTLE (82804-984-11) 82804-984-30 30 TABLET in 1 BOTTLE (82804-984-30) 82804-984-55 500 TABLET in 1 BOTTLE (82804-984-55) 82804-984-60 60 TABLET in 1 BOTTLE (82804-984-60) 82804-984-90 90 TABLET in 1 BOTTLE (82804-984-90)

Ingredients (1)

phenobarbital (64.8 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": "6b5ca781-50a9-4e89-8184-831c7c2936b2", "openfda": {"upc": ["0382804984305", "0382804982301", "0382804983308", "0382804985302"], "unii": ["YQE403BP4D"], "rxcui": ["198086", "199164", "199167", "199168"], "spl_set_id": ["6b5ca781-50a9-4e89-8184-831c7c2936b2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82804-984-00)", "package_ndc": "82804-984-00", "marketing_start_date": "20241028"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (82804-984-11)", "package_ndc": "82804-984-11", "marketing_start_date": "20241028"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-984-30)", "package_ndc": "82804-984-30", "marketing_start_date": "20241028"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82804-984-55)", "package_ndc": "82804-984-55", "marketing_start_date": "20241028"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-984-60)", "package_ndc": "82804-984-60", "marketing_start_date": "20241028"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-984-90)", "package_ndc": "82804-984-90", "marketing_start_date": "20241028"}], "brand_name": "Phenobarbital", "product_id": "82804-984_6b5ca781-50a9-4e89-8184-831c7c2936b2", "dosage_form": "TABLET", "product_ndc": "82804-984", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "64.8 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20230908", "listing_expiration_date": "20261231"}