Home NDC 0409-4916-34 Sodium Bicarbonate
Product NDC 0409-4916
Requested package NDC 0409-4916-34
11-digit product format 004094916
Labeler code 0409
Product ID 0409-4916_6404d8a8-4b75-4c19-8085-d5892343925e
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name SODIUM BICARBONATE
Dosage form INJECTION, SOLUTION
Route INTRAVENOUS
Labeler Hospira, Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2006-02-16
Marketing end 2022-02-01
Substance SODIUM BICARBONATE
Active strength 75 mg/mL
NDC exclude flag No
Listing certified through 0000-00-00
Current FDA listing Historical FDA.report record 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 · 12 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 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…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…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0409-4916-14 Sodium Bicarbonate 1 in 1 CARTON INJECTION, SOLUTION 1 8 0409-4916-14 Sodium Bicarbonate 10 in 1 PACKAGE INJECTION, SOLUTION 10 8 0409-4916-24 Sodium Bicarbonate 50 mL in 1 SYRINGE INJECTION, SOLUTION 50 8
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM BICARBONATE ACTIVE INGREDIENT 8MDF5V39QO SODIUM BICARBONATE INJECTION, SOLUTION [HOSPIRA, INC.] 1 Sodium Bicarbonate ACTIVE INGREDIENT 8MDF5V39QO SODIUM BICARBONATE INJECTION [GENERAL INJECTABLES & VACCINES, INC.] 1 BICARBONATE ION ACTIVE MOIETY HN1ZRA3Q20 SODIUM BICARBONATE INJECTION, SOLUTION [HOSPIRA, INC.] 1 Sodium Cation ACTIVE MOIETY LYR4M0NH37 SODIUM BICARBONATE INJECTION [GENERAL INJECTABLES & VACCINES, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R SODIUM BICARBONATE INJECTION, SOLUTION [HOSPIRA, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0409-4916 SODIUM BICARBONATE INJECTION, SOLUTION [HOSPIRA, INC.] 7 Legacy NDC, 3 package rows 20241220_ea20a5eb-641e-48cd-bcfa-74c04c45dfda.zip
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 Marketing end Sample Exclude flag Status 0409-4916-34 00409491634 10 CARTON in 1 PACKAGE (0409-4916-34) > 1 SYRINGE in 1 CARTON > 50 mL in 1 SYRINGE 10 carton 2006-02-16 2022-02-01 No No Current