POTASSIUM CHLORIDE
- Product NDC
- 63629-1077
- 11-digit product format
- 636291077
- Labeler code
- 63629
- Product ID
- 63629-1077_4af1a359-6c99-4828-b384-c9ec49843369
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- POTASSIUM CHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208864
- Marketing category
- ANDA
- Marketing start
- 2020-06-17
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 600 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1077-1 | 63629107701 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-1077-1) | 2020-06-17 | 0000-00-00 | No | No | Current |
| 63629-1077-2 | 63629107702 | 360 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-1077-2) | 2020-06-17 | 0000-00-00 | No | No | Current |