NDC product
Glycopyrrolate Oral Solution
NDC 51672-5316 · Sun Pharmaceutical Industries, Inc.
Key facts
| Product NDC | 51672-5316 |
|---|---|
| Proprietary name | Glycopyrrolate Oral Solution |
| Nonproprietary name | Glycopyrrolate Oral Solution |
| Substances | GLYCOPYRROLATE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA212467 |
| Pharmacologic classes | Anticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
| Marketing start | Jul 5, 2022 |
| 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: