phenobarbital

Generic: phenobarbital

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenobarbital
Generic Name phenobarbital
Labeler westminster pharmaceuticals, llc
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

phenobarbital 20 mg/5mL

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-357
Product ID 69367-357_829b32b5-8c54-455c-83cb-d8dfb7d4407f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2023-10-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367357
Hyphenated Format 69367-357

Supplemental Identifiers

RxCUI
702519
UNII
YQE403BP4D

Packaging Origin

Original Packager
true

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
  • 20 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (69367-357-16)
source: ndc

Packages (1)

69367-357-16 473 mL in 1 BOTTLE (69367-357-16)

Ingredients (1)

phenobarbital (20 mg/5mL)

Linked Drug Pages (1)

Phenobarbital ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "829b32b5-8c54-455c-83cb-d8dfb7d4407f", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["702519"], "spl_set_id": ["0ca8847d-1966-47a0-995e-a5c0d2fd699d"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (69367-357-16)", "package_ndc": "69367-357-16", "marketing_start_date": "20231013"}], "brand_name": "Phenobarbital", "product_id": "69367-357_829b32b5-8c54-455c-83cb-d8dfb7d4407f", "dosage_form": "LIQUID", "product_ndc": "69367-357", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "20 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20231013", "listing_expiration_date": "20261231"}