NDC product
Hydrocodone Bitartrate and Acetaminophen
NDC 27808-049 · Cranbury Pharmaceuticals, LLC
Key facts
| Product NDC | 27808-049 |
|---|---|
| Proprietary name | Hydrocodone Bitartrate and Acetaminophen |
| Nonproprietary name | Hydrocodone Bitartrate and Acetaminophen |
| Substances | HYDROCODONE BITARTRATE, ACETAMINOPHEN |
| Dosage form | SOLUTION |
| Route | ORAL |
| Labeler | Cranbury Pharmaceuticals, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA201295 |
| DEA schedule | CII |
| Pharmacologic classes | Opioid Agonist [EPC], Opioid Agonists [MoA] |
| Marketing start | Dec 30, 2021 |
| 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: