Hyperlyte
- Product NDC
- 0264-1943
- 11-digit product format
- 002641943
- Labeler code
- 0264
- Product ID
- 0264-1943_04fffe7e-5bee-4824-a5e4-b1f8b8d1f811
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Multi Electrolyte Concentrate
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- B. Braun Medical Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-04-12
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM ACETATE; SODIUM CHLORIDE; SODIUM ACETATE; MAGNESIUM CHLORIDE; CALCIUM CHLORIDE
- Active strength
- 2 g/20mL; g/20mL; g/20mL; g/20mL; g/20mL
- 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],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0264-1943-20 | 00264194320 | 12 CONTAINER in 1 CASE (0264-1943-20) > 250 mL in 1 CONTAINER | 12 container | 2012-04-12 | 0000-00-00 | No | No | Current |