NDC product
Doxycycline Monohydrate
NDC 62135-263 · Chartwell RX, LLC.
Key facts
| Product NDC | 62135-263 |
|---|---|
| Proprietary name | Doxycycline Monohydrate |
| Nonproprietary name | Doxycycline Monohydrate |
| Substances | DOXYCYCLINE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | Chartwell RX, LLC. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA050641 |
| Pharmacologic classes | Tetracycline-class Drug [EPC], Tetracyclines [CS] |
| Marketing start | Dec 29, 1989 |
| 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: