Home NDC 24689-137 Sodium Bicarbonate
Product NDC 24689-137
11-digit product format 246890137
Labeler code 24689
Product ID 24689-137_08352100-b59d-c799-e063-6294a90a5e3b
Type HUMAN OTC DRUG
Nonproprietary name Sodium Bicarbonate
Dosage form TABLET
Route ORAL
Labeler APNAR PHARMA LP
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-06-24
Substance SODIUM BICARBONATE
Active strength 650 mg/1
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Sodium Bicarbonate
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM BICARBONATE 650 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8MDF5V39QO Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198861 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 24689-137-01 Sodium Bicarbonate 1000 in 1 BOTTLE TABLET 1000 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 24689-137 SODIUM BICARBONATE TABLET [APNAR PHARMA LP] 4 Current NDC, Legacy NDC, 1 package rows 20231021_e206c240-55c2-2d00-e053-2a95a90a1779.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 8 of 34 · 678 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 24689-137-01 24689013701 1000 TABLET in 1 BOTTLE (24689-137-01) 1000 tablet 2022-06-24 0000-00-00 No No Current