NDC product
DICYCLOMINE HYDROCHLORIDE
NDC 73473-800 · Solaris Pharma Corporation
Key facts
| Product NDC | 73473-800 |
|---|---|
| Proprietary name | DICYCLOMINE HYDROCHLORIDE |
| Nonproprietary name | DICYCLOMINE HYDROCHLORIDE |
| Substances | DICYCLOMINE HYDROCHLORIDE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | Solaris Pharma Corporation |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA216639 |
| Pharmacologic classes | Anticholinergic [EPC], Cholinergic Antagonists [MoA] |
| Marketing start | Jun 10, 2025 |
| 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: