pentobarbital sodium

Generic: pentobarbital sodium

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pentobarbital sodium
Generic Name pentobarbital sodium
Labeler sagent pharmaceuticals
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

pentobarbital sodium 50 mg/mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-676
Product ID 25021-676_5eb44748-b3d4-4d86-a172-9f03eb804671
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206404
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2017-04-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021676
Hyphenated Format 25021-676

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 ANDA206404 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (25021-676-20) / 20 mL in 1 VIAL
  • 1 VIAL in 1 CARTON (25021-676-50) / 50 mL in 1 VIAL
source: ndc

Packages (2)

25021-676-20 1 VIAL in 1 CARTON (25021-676-20) / 20 mL in 1 VIAL 25021-676-50 1 VIAL in 1 CARTON (25021-676-50) / 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": "5eb44748-b3d4-4d86-a172-9f03eb804671", "openfda": {"unii": ["NJJ0475N0S"], "rxcui": ["238090"], "spl_set_id": ["e9f4b344-b092-4eec-b49d-d8cfe8ebc05d"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-676-20)  / 20 mL in 1 VIAL", "package_ndc": "25021-676-20", "marketing_start_date": "20170419"}, {"sample": false, "description": "1 VIAL in 1 CARTON (25021-676-50)  / 50 mL in 1 VIAL", "package_ndc": "25021-676-50", "marketing_start_date": "20170419"}], "brand_name": "pentobarbital sodium", "product_id": "25021-676_5eb44748-b3d4-4d86-a172-9f03eb804671", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "25021-676", "dea_schedule": "CII", "generic_name": "pentobarbital sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "pentobarbital sodium", "active_ingredients": [{"name": "PENTOBARBITAL SODIUM", "strength": "50 mg/mL"}], "application_number": "ANDA206404", "marketing_category": "ANDA", "marketing_start_date": "20170419", "listing_expiration_date": "20261231"}