NDC product
Benztropine Mesylate
NDC 68084-381 · American Health Packaging
Key facts
| Product NDC | 68084-381 |
|---|---|
| Proprietary name | Benztropine Mesylate |
| Nonproprietary name | Benztropine Mesylate |
| Substances | BENZTROPINE MESYLATE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | American Health Packaging |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA040715 |
| Pharmacologic classes | Anticholinergic [EPC], Antihistamine [EPC], Cholinergic Antagonists [MoA], Histamine Receptor Antagonists [MoA] |
| Marketing start | Nov 9, 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: