Home NDC 72162-1330-2 Phenobarbital Sodium
Product NDC 72162-1330
Requested package NDC 72162-1330-2
11-digit product format 721621330
Labeler code 72162
Product ID 72162-1330_373e94d6-7bdc-de9b-e063-6294a90af333
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Phenobarbital Sodium
Dosage form INJECTION
Route INTRAMUSCULAR
Labeler Bryant Ranch Prepack
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2020-02-05
Substance PHENOBARBITAL SODIUM
Active strength 130 mg/mL
DEA schedule CIV
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…
Additional Listing Data#
Finished product Yes
Brand name base Phenobarbital Sodium
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PHENOBARBITAL SODIUM 130 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SW9M9BB5K3 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2671204 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72162-1330-2 Phenobarbital Sodium 3 in 1 BOX, UNIT-DOSE INJECTION 3 109 72162-1330-4 Phenobarbital Sodium 25 in 1 BOX, UNIT-DOSE INJECTION 25 109 72162-1330-6 Phenobarbital Sodium 1 mL in 1 VIAL INJECTION 1 109 72162-1330-8 Phenobarbital Sodium 1 mL in 1 VIAL INJECTION 1 109
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72162-1330-2 72162133002 3 VIAL in 1 BOX, UNIT-DOSE (72162-1330-2) / 1 mL in 1 VIAL (72162-1330-8) 3 vial 2024-04-08 No No Current