NDC product
Doxycycline
NDC 71288-030 · Meitheal Pharmaceuticals Inc.
Key facts
| Product NDC | 71288-030 |
|---|---|
| Proprietary name | Doxycycline |
| Nonproprietary name | Doxycycline |
| Substances | DOXYCYCLINE HYCLATE |
| Dosage form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route | INTRAVENOUS |
| Labeler | Meitheal Pharmaceuticals Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA218053 |
| Pharmacologic classes | Tetracycline-class Drug [EPC], Tetracyclines [CS] |
| Marketing start | Oct 28, 2024 |
| 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: