NDC product
Hydrocodone Polistirex and Chlorpheniramine Polistirex extended-release
NDC 27808-086 · Cranbury Pharmaceuticals, LLC
Key facts
| Product NDC | 27808-086 |
|---|---|
| Proprietary name | Hydrocodone Polistirex and Chlorpheniramine Polistirex |
| Nonproprietary name | Hydrocodone Polistirex and Chlorpheniramine Polistirex |
| Substances | HYDROCODONE BITARTRATE, CHLORPHENIRAMINE MALEATE |
| Dosage form | SUSPENSION, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | Cranbury Pharmaceuticals, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA091632 |
| DEA schedule | CII |
| Pharmacologic classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Opioid Agonist [EPC], Opioid Agonists [MoA] |
| Marketing start | Mar 6, 2015 |
| Listing certified through | Dec 31, 2027 |
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: