NDC product
Endopan HP
NDC 44911-0598 · Energique, Inc.
Key facts
| Product NDC | 44911-0598 |
|---|---|
| Proprietary name | Endopan HP |
| Nonproprietary name | Aceticum Acidum, Colchicum Autumnale, Lacticum Acidum, Lycopodium Clavatum, Phosphoricum Acidum, Phosphorus, Syzygium Jambolanum, Uranium Nitricum |
| Substances | ACETIC ACID, COLCHICUM AUTUMNALE BULB, LACTIC ACID, DL-, LYCOPODIUM CLAVATUM SPORE, PHOSPHORIC ACID, PHOSPHORUS, SYZYGIUM CUMINI SEED, URANYL NITRATE HEXAHYDRATE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Energique, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | May 24, 2021 |
| Marketing end | Jun 9, 2028 |
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