Details for New Drug Application (NDA): 017058
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The generic ingredient in METHADONE HYDROCHLORIDE is methadone hydrochloride. There are thirteen drug master file entries for this compound. Seventeen suppliers are listed for this compound. Additional details are available on the methadone hydrochloride profile page.
Summary for 017058
Tradename: | METHADONE HYDROCHLORIDE |
Applicant: | Hikma |
Ingredient: | methadone hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 017058
Mechanism of Action | Full Opioid Agonists |
Medical Subject Heading (MeSH) Categories for 017058
Suppliers and Packaging for NDA: 017058
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
METHADONE HYDROCHLORIDE | methadone hydrochloride | TABLET, FOR SUSPENSION;ORAL | 017058 | NDA | Hikma Pharmaceuticals USA Inc. | 0054-4538 | 0054-4538-25 | 100 TABLET in 1 BOTTLE, PLASTIC (0054-4538-25) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, FOR SUSPENSION;ORAL | Strength | 40MG | ||||
Approval Date: | Approved Prior to Jan 1, 1982 | TE: | AA | RLD: | Yes |
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