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 100 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-851
Product ID 71205-851_6cf88fef-0c82-4d5d-85e8-5896ac013165
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2020-11-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205851
Hyphenated Format 71205-851

Supplemental Identifiers

RxCUI
198083 198089 312357
UPC
0371205851309 0371205848309 0371205845308
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
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (71205-851-00)
  • 1000 TABLET in 1 BOTTLE (71205-851-11)
  • 30 TABLET in 1 BOTTLE (71205-851-30)
  • 500 TABLET in 1 BOTTLE (71205-851-55)
  • 60 TABLET in 1 BOTTLE (71205-851-60)
  • 240 TABLET in 1 BOTTLE (71205-851-64)
  • 120 TABLET in 1 BOTTLE (71205-851-72)
  • 180 TABLET in 1 BOTTLE (71205-851-78)
  • 90 TABLET in 1 BOTTLE (71205-851-90)
source: ndc

Packages (9)

71205-851-00 100 TABLET in 1 BOTTLE (71205-851-00) 71205-851-11 1000 TABLET in 1 BOTTLE (71205-851-11) 71205-851-30 30 TABLET in 1 BOTTLE (71205-851-30) 71205-851-55 500 TABLET in 1 BOTTLE (71205-851-55) 71205-851-60 60 TABLET in 1 BOTTLE (71205-851-60) 71205-851-64 240 TABLET in 1 BOTTLE (71205-851-64) 71205-851-72 120 TABLET in 1 BOTTLE (71205-851-72) 71205-851-78 180 TABLET in 1 BOTTLE (71205-851-78) 71205-851-90 90 TABLET in 1 BOTTLE (71205-851-90)

Ingredients (1)

phenobarbital (100 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": "6cf88fef-0c82-4d5d-85e8-5896ac013165", "openfda": {"upc": ["0371205851309", "0371205848309", "0371205845308"], "unii": ["YQE403BP4D"], "rxcui": ["198083", "198089", "312357"], "spl_set_id": ["6cf88fef-0c82-4d5d-85e8-5896ac013165"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71205-851-00)", "package_ndc": "71205-851-00", "marketing_start_date": "20230213"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71205-851-11)", "package_ndc": "71205-851-11", "marketing_start_date": "20230213"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-851-30)", "package_ndc": "71205-851-30", "marketing_start_date": "20230213"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71205-851-55)", "package_ndc": "71205-851-55", "marketing_start_date": "20230213"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-851-60)", "package_ndc": "71205-851-60", "marketing_start_date": "20230213"}, {"sample": false, "description": "240 TABLET in 1 BOTTLE (71205-851-64)", "package_ndc": "71205-851-64", "marketing_start_date": "20230213"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71205-851-72)", "package_ndc": "71205-851-72", "marketing_start_date": "20230213"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71205-851-78)", "package_ndc": "71205-851-78", "marketing_start_date": "20230213"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-851-90)", "package_ndc": "71205-851-90", "marketing_start_date": "20230213"}], "brand_name": "Phenobarbital", "product_id": "71205-851_6cf88fef-0c82-4d5d-85e8-5896ac013165", "dosage_form": "TABLET", "product_ndc": "71205-851", "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": "100 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20201101", "listing_expiration_date": "20261231"}