Details for New Drug Application (NDA): 213906
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The generic ingredient in LEVORPHANOL TARTRATE is levorphanol tartrate. There are six drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the levorphanol tartrate profile page.
Summary for 213906
Tradename: | LEVORPHANOL TARTRATE |
Applicant: | Sun Pharm Inds Inc |
Ingredient: | levorphanol tartrate |
Patents: | 0 |
Pharmacology for NDA: 213906
Mechanism of Action | Full Opioid Agonists |
Medical Subject Heading (MeSH) Categories for 213906
Suppliers and Packaging for NDA: 213906
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
LEVORPHANOL TARTRATE | levorphanol tartrate | TABLET;ORAL | 213906 | ANDA | Sun Pharmaceutical Industries, Inc. | 57664-058 | 57664-058-88 | 100 TABLET in 1 BOTTLE (57664-058-88) |
LEVORPHANOL TARTRATE | levorphanol tartrate | TABLET;ORAL | 213906 | ANDA | Sun Pharmaceutical Industries, Inc. | 57664-762 | 57664-762-88 | 100 TABLET in 1 BOTTLE (57664-762-88) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 2MG | ||||
Approval Date: | Jun 17, 2021 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 3MG | ||||
Approval Date: | Apr 25, 2023 | TE: | AB | RLD: | No |
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