NDC product
Cyclomydril
NDC 0065-0359 · Alcon Laboratories, Inc.
Key facts
| Product NDC | 0065-0359 |
|---|---|
| Proprietary name | Cyclomydril |
| Nonproprietary name | cyclopentolate hydrochloride and phenylephrine hydrochloride |
| Substances | CYCLOPENTOLATE HYDROCHLORIDE, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage form | SOLUTION/ DROPS |
| Route | OPHTHALMIC |
| Labeler | Alcon Laboratories, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA084300 |
| Pharmacologic classes | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
| Marketing start | Jun 30, 1958 |
| 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: