Potassium Chloride
- Product NDC
- 0574-0180
- 11-digit product format
- 005740180
- Labeler code
- 0574
- Product ID
- 0574-0180_8847c3c5-cff9-46e6-986e-08a80f5383d6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Paddock Laboratories, LLC
- Application
- ANDA200185
- Marketing category
- ANDA
- Marketing start
- 2011-06-03
- Marketing end
- 2020-03-01
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 600 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record