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 30 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-890
Product ID 71205-890_886f2c7d-6a6e-4d73-bbbd-61cff9514a87
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 71205890
Hyphenated Format 71205-890

Supplemental Identifiers

RxCUI
312362
UPC
0371205890308
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
  • 30 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (71205-890-00)
  • 1000 TABLET in 1 BOTTLE (71205-890-11)
  • 30 TABLET in 1 BOTTLE (71205-890-30)
  • 500 TABLET in 1 BOTTLE (71205-890-55)
  • 60 TABLET in 1 BOTTLE (71205-890-60)
  • 90 TABLET in 1 BOTTLE (71205-890-90)
source: ndc

Packages (6)

Ingredients (1)

phenobarbital (30 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "886f2c7d-6a6e-4d73-bbbd-61cff9514a87", "openfda": {"upc": ["0371205890308"], "unii": ["YQE403BP4D"], "rxcui": ["312362"], "spl_set_id": ["8fd2647b-6c3a-4b4c-a93b-304be364baf3"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71205-890-00)", "package_ndc": "71205-890-00", "marketing_start_date": "20210803"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71205-890-11)", "package_ndc": "71205-890-11", "marketing_start_date": "20210803"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-890-30)", "package_ndc": "71205-890-30", "marketing_start_date": "20210803"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71205-890-55)", "package_ndc": "71205-890-55", "marketing_start_date": "20210803"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-890-60)", "package_ndc": "71205-890-60", "marketing_start_date": "20210803"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-890-90)", "package_ndc": "71205-890-90", "marketing_start_date": "20210803"}], "brand_name": "Phenobarbital", "product_id": "71205-890_886f2c7d-6a6e-4d73-bbbd-61cff9514a87", "dosage_form": "TABLET", "product_ndc": "71205-890", "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": "30 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20201101", "listing_expiration_date": "20261231"}