NDC product
Chlordiazepoxide and Amitriptyline Hydrochloride
NDC 0378-0277 · Mylan Pharmaceuticals Inc.
Key facts
| Product NDC | 0378-0277 |
|---|---|
| Proprietary name | Chlordiazepoxide and Amitriptyline Hydrochloride |
| Nonproprietary name | chlordiazepoxide and amitriptyline hydrochloride |
| Substances | CHLORDIAZEPOXIDE, AMITRIPTYLINE HYDROCHLORIDE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Mylan Pharmaceuticals Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA071297 |
| DEA schedule | CIV |
| Pharmacologic classes | Benzodiazepine [EPC], Benzodiazepines [CS], Tricyclic Antidepressant [EPC] |
| Marketing start | Dec 10, 1986 |
| 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: