NDC product
Perikabiven
NDC 63323-714 · Fresenius Kabi USA, LLC
Key facts
| Product NDC | 63323-714 |
|---|---|
| Proprietary name | Perikabiven |
| Nonproprietary name | Dextrose, Soybean oil, Electrolytes, Lysine, Phenylalanine, Leucine, Valine, Threonine, Methionine, Isoleucine, Tryptophan, Alanine and 7 more |
| Substances | DEXTROSE MONOHYDRATE, SOYBEAN OIL, SODIUM ACETATE, POTASSIUM CHLORIDE, SODIUM GLYCEROPHOSPHATE ANHYDROUS, MAGNESIUM SULFATE HEPTAHYDRATE, CALCIUM CHLORIDE, LYSINE HYDROCHLORIDE, PHENYLALANINE, LEUCINE, VALINE, HISTIDINE and 12 more |
| Dosage form | INJECTION, EMULSION |
| Route | INTRAVENOUS |
| Labeler | Fresenius Kabi USA, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA200656 |
| Pharmacologic classes | Amino Acid [EPC], Amino Acids [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations and 15 more |
| Marketing start | Aug 25, 2014 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: