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