Product NDC: | 0054-0438 |
Proprietary Name: | LEVORPHANOL TARTRATE |
Non Proprietary Name: | LEVORPHANOL TARTRATE |
Active Ingredient(s): | 2 mg/1 & nbsp; LEVORPHANOL TARTRATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0054-0438 |
Labeler Name: | Roxane Laboratories, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074278 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000331 |
Package NDC: | 0054-0438-25 |
Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0054-0438-25) |
NDC Code | 0054-0438-25 |
Proprietary Name | LEVORPHANOL TARTRATE |
Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0054-0438-25) |
Product NDC | 0054-0438 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | LEVORPHANOL TARTRATE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20000331 |
Marketing Category Name | ANDA |
Labeler Name | Roxane Laboratories, Inc |
Substance Name | LEVORPHANOL TARTRATE |
Strength Number | 2 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |