phenobarbital
Generic: phenobarbital
Labeler: quagen pharmaceuticals llcDrug Facts
Product Profile
Brand Name
phenobarbital
Generic Name
phenobarbital
Labeler
quagen pharmaceuticals llc
Dosage Form
TABLET
Routes
Active Ingredients
phenobarbital 64.8 mg/1
Manufacturer
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
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 64.8 mg/1
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)
Packages (3)
Ingredients (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"}