pentobarbital sodium

Generic: pentobarbital sodium

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pentobarbital sodium
Generic Name pentobarbital sodium
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

pentobarbital sodium 50 mg/mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 24201-010
Product ID 24201-010_092d00fe-9f8a-47ea-b9bc-07ef41d2b418
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203619
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2025-10-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24201010
Hyphenated Format 24201-010

Supplemental Identifiers

RxCUI
238090
UNII
NJJ0475N0S

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 pentobarbital sodium (source: ndc)
Generic Name pentobarbital sodium (source: ndc)
Application Number ANDA203619 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (24201-010-20) / 20 mL in 1 VIAL
  • 1 VIAL in 1 CARTON (24201-010-50) / 50 mL in 1 VIAL
source: ndc

Packages (2)

24201-010-20 1 VIAL in 1 CARTON (24201-010-20) / 20 mL in 1 VIAL 24201-010-50 1 VIAL in 1 CARTON (24201-010-50) / 50 mL in 1 VIAL

Ingredients (1)

pentobarbital sodium (50 mg/mL)

Linked Drug Pages (1)

Pentobarbital Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "092d00fe-9f8a-47ea-b9bc-07ef41d2b418", "openfda": {"unii": ["NJJ0475N0S"], "rxcui": ["238090"], "spl_set_id": ["d375b92a-baa1-4d63-9ad1-1467dcfde7d5"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (24201-010-20)  / 20 mL in 1 VIAL", "package_ndc": "24201-010-20", "marketing_start_date": "20251001"}, {"sample": false, "description": "1 VIAL in 1 CARTON (24201-010-50)  / 50 mL in 1 VIAL", "package_ndc": "24201-010-50", "marketing_start_date": "20251001"}], "brand_name": "Pentobarbital Sodium", "product_id": "24201-010_092d00fe-9f8a-47ea-b9bc-07ef41d2b418", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "24201-010", "dea_schedule": "CII", "generic_name": "Pentobarbital Sodium", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pentobarbital Sodium", "active_ingredients": [{"name": "PENTOBARBITAL SODIUM", "strength": "50 mg/mL"}], "application_number": "ANDA203619", "marketing_category": "ANDA", "marketing_start_date": "20251001", "listing_expiration_date": "20271231"}