Sodium Bicarbonate

Product NDC
0904-7261
11-digit product format
009047261
Labeler code
0904
Product ID
0904-7261_289e96ec-d8d1-ee93-e063-6394a90a38d7
Type
HUMAN OTC DRUG
Nonproprietary name
Sodium Bicarbonate
Dosage form
TABLET
Route
ORAL
Labeler
Major Pharmaceuticals
Application
M001
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-10-26
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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
8MDF5V39QOSODIUM BICARBONATE144-55-8SODIUM BICARBONATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
0904-7261-610090472616110 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-7261-61) / 10 TABLET in 1 BLISTER PACK10 blister pack2022-10-26NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Sodium BicarbonateCardinal Health 107, LLC2025-10-29HUMAN OTC DRUG LABEL4
4624 - MajorMajor Pharmaceuticals2024-12-06HUMAN OTC DRUG LABEL2
4624 - MajorCardinal Health 107, LLC2024-10-10HUMAN OTC DRUG LABEL3