Potassium Chloride
- Product NDC
- 68071-5002
- 11-digit product format
- 680715002
- Labeler code
- 68071
- Product ID
- 68071-5002_bbb32fa7-6047-5010-e053-2a95a90ae159
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA210733
- Marketing category
- ANDA
- Marketing start
- 2018-08-31
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 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
- 2022-12-31
- 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 |
|---|
| 68071-5002-9 | 68071500209 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-5002-9) | 2019-07-29 | 0000-00-00 | No | No | Current |