phenobarbital

Generic: phenobarbital

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

Drug Facts

Product Profile

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

phenobarbital 64.8 mg/1

Manufacturer
QUAGEN PHARMACEUTICALS LLC

Identifiers & Regulatory

Product NDC 70752-163
Product ID 70752-163_234e0cf8-e1c9-47a2-8fa3-8a4db929c866
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2020-09-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70752163
Hyphenated Format 70752-163

Supplemental Identifiers

RxCUI
198086 199164 199167 199168
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
  • 64.8 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70752-163-10)
  • 1000 TABLET in 1 BOTTLE (70752-163-11)
  • 500 TABLET in 1 BOTTLE (70752-163-14)
source: ndc

Packages (3)

Ingredients (1)

phenobarbital (64.8 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "234e0cf8-e1c9-47a2-8fa3-8a4db929c866", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198086", "199164", "199167", "199168"], "spl_set_id": ["7e6853a4-478d-40e3-b041-4cff02a74c8c"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70752-163-10)", "package_ndc": "70752-163-10", "marketing_start_date": "20200915"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70752-163-11)", "package_ndc": "70752-163-11", "marketing_start_date": "20200915"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70752-163-14)", "package_ndc": "70752-163-14", "marketing_start_date": "20200915"}], "brand_name": "PHENOBARBITAL", "product_id": "70752-163_234e0cf8-e1c9-47a2-8fa3-8a4db929c866", "dosage_form": "TABLET", "product_ndc": "70752-163", "dea_schedule": "CIV", "generic_name": "PHENOBARBITAL", "labeler_name": "QUAGEN PHARMACEUTICALS LLC", "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": "20200915", "listing_expiration_date": "20261231"}