Potassium Bicarbonate

Product NDC
0245-0039
11-digit product format
002450039
Labeler code
0245
Product ID
0245-0039_213fd739-e9f9-437d-807c-2caf3b8212de
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium Bicarbonate
Dosage form
TABLET, EFFERVESCENT
Route
ORAL
Labeler
Upsher-Smith Laboratories, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2014-09-01
Marketing end
0000-00-00
Substance
POTASSIUM BICARBONATE
Active strength
978 mg/1
Pharmacologic classes
Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0245-0039-01EA - Each0245-003910ee5bf9-afea-4f52-bc06-ea960a1bee8e12013-02-13
0245-0039-30EA - Each0245-003902f168d3-7c72-46e1-8036-f433e3bd6e4112013-02-13