Potassium Chloride
- Product NDC
- 0574-0181
- 11-digit product format
- 005740181
- Labeler code
- 0574
- Product ID
- 0574-0181_a70f3a95-8160-4905-8dbb-50ea5ba6e1ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Padagis US LLC
- Application
- ANDA200185
- Marketing category
- ANDA
- Marketing start
- 2011-06-03
- 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
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0574-0181-01 | 00574018101 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0574-0181-01) | 2011-06-03 | 0000-00-00 | No | No | Current |
| 0574-0181-05 | 00574018105 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0574-0181-05) | 2011-06-03 | 0000-00-00 | No | No | Current |