Potassium Chloride Extended-release
- Product NDC
- 0904-7201
- 11-digit product format
- 009047201
- Labeler code
- 0904
- Product ID
- 0904-7201_e635733b-b1b7-4aa8-b23e-693248c19df7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride Extended-release
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA214452
- Marketing category
- ANDA
- Marketing start
- 2021-01-30
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7201-61 | 00904720161 | 100 BLISTER PACK in 1 CARTON (0904-7201-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2021-01-30 | 0000-00-00 | No | No | Current |