POTASSIUM CHLORIDE
- Product NDC
- 0264-1940
- 11-digit product format
- 002641940
- Labeler code
- 0264
- Product ID
- 0264-1940_25b5b95b-5ac5-4e79-baed-44aaa1263e0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- POTASSIUM CHLORIDE
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- PARENTERAL
- Labeler
- B. Braun Medical Inc.
- Application
- ANDA085870
- Marketing category
- ANDA
- Marketing start
- 1978-03-21
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 15 g/100mL
- 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 |
|---|
| 0264-1940-20 | 00264194020 | 12 CONTAINER in 1 CASE (0264-1940-20) > 250 mL in 1 CONTAINER | 12 container | 1978-03-21 | 0000-00-00 | No | No | Current |