NDC product
Acetylcholine Chloride
NDC 43742-0817 · Deseret Biologicals, Inc.
Key facts
| Product NDC | 43742-0817 |
|---|---|
| Proprietary name | Acetylcholine Chloride |
| Nonproprietary name | Acetylcholine Chloride |
| Substances | ACETYLCHOLINE CHLORIDE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Deseret Biologicals, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Cholinergic Agonists [MoA], Cholinergic Receptor Agonist [EPC] |
| Marketing start | Jul 21, 2016 |
| Marketing end | Sep 15, 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