phenobarbital
Generic: phenobarbital
Labeler: taro pharmaceuticals u.s.a. inc.Drug Facts
Product Profile
Brand Name
phenobarbital
Generic Name
phenobarbital
Labeler
taro pharmaceuticals u.s.a. inc.
Dosage Form
TABLET
Routes
Active Ingredients
phenobarbital 15 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51672-5331
Product ID
51672-5331_bc2d569d-e2c5-4a94-b259-cac1fcc6cdf4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2024-08-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516725331
Hyphenated Format
51672-5331
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
- 15 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (51672-5331-1)
- 1000 TABLET in 1 BOTTLE, PLASTIC (51672-5331-3)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bc2d569d-e2c5-4a94-b259-cac1fcc6cdf4", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198083", "198086", "198089", "199164", "199167", "199168", "312357", "312362"], "spl_set_id": ["fa09b4f2-edb0-4594-a2d2-b16f7b9686b4"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A. Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (51672-5331-1)", "package_ndc": "51672-5331-1", "marketing_start_date": "20240801"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (51672-5331-3)", "package_ndc": "51672-5331-3", "marketing_start_date": "20240801"}], "brand_name": "Phenobarbital", "product_id": "51672-5331_bc2d569d-e2c5-4a94-b259-cac1fcc6cdf4", "dosage_form": "TABLET", "product_ndc": "51672-5331", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Taro Pharmaceuticals U.S.A. Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "15 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240801", "listing_expiration_date": "20261231"}