Potassium Chloride
- Product NDC
- 63629-6430
- 11-digit product format
- 636296430
- Labeler code
- 63629
- Product ID
- 63629-6430_7d0591be-ba83-4316-8328-74fcb2029bd2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074726
- Marketing category
- ANDA
- Marketing start
- 1998-11-20
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 1500 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6430-1 | 63629643001 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-6430-1) | 2015-08-28 | 0000-00-00 | No | No | Current |
| 63629-6430-2 | 63629643002 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-6430-2) | 2015-09-02 | 0000-00-00 | No | No | Current |