Drug application
METHADONE HYDROCHLORIDE (METHADONE HYDROCHLORIDE)
Drugs@FDA NDA 006383 · MALLINCKRODT INC
Key facts
| Drug name | METHADONE HYDROCHLORIDE |
|---|---|
| Active ingredients | METHADONE HYDROCHLORIDE |
| Application type | NDA |
| Application number | 006383 |
| Company | MALLINCKRODT INC |
| Dosage forms | POWDER, FOR RX COMPOUNDING |
| Strength | 50GM/BOT |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Dec 15, 1947 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- 1–9 Label versions
- 1–9 Products
- None Therapeutic equivalents
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: