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LEVORPHANOL TARTRATE - 0054-0438-25 - (LEVORPHANOL TARTRATE)

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Drug Information of LEVORPHANOL TARTRATE

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)

Labeler Information of LEVORPHANOL TARTRATE

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 Information of LEVORPHANOL TARTRATE

Package NDC: 0054-0438-25
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0054-0438-25)

NDC Information of LEVORPHANOL TARTRATE

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]

Complete Information of LEVORPHANOL TARTRATE


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