NDC product
Bactimicina Childrens Cough and Cold
NDC 24286-1551 · DLC Laboratories, Inc.
Key facts
| Product NDC | 24286-1551 |
|---|---|
| Proprietary name | Bactimicina Childrens Cough and Cold |
| Nonproprietary name | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE |
| Substances | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | DLC Laboratories, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] |
| Marketing start | Oct 23, 2009 |
| 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: