Visitor Monitoring Drug Details: MEPERIDINE HYDROCHLORIDE
 
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Drug Details

Drug Name: MEPERIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 080455
Active Ingredient(s): MEPERIDINE HYDROCHLORIDE
Company: BAXTER HLTHCARE CORP
Original Approval or Tentative Approval Date: April 26, 1972
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
MEPERIDINE HYDROCHLORIDE MEPERIDINE HYDROCHLORIDE25MG/MLINJECTABLE; INJECTION Prescription No AP
MEPERIDINE HYDROCHLORIDE MEPERIDINE HYDROCHLORIDE50MG/MLINJECTABLE; INJECTION Prescription No AP
MEPERIDINE HYDROCHLORIDE MEPERIDINE HYDROCHLORIDE75MG/MLINJECTABLE; INJECTION Prescription No AP
MEPERIDINE HYDROCHLORIDE MEPERIDINE HYDROCHLORIDE100MG/MLINJECTABLE; INJECTION Prescription No AP


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