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Fentanyl Citrate - 10019-037-25 - (Fentanyl Citrate)

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Drug Information of Fentanyl Citrate

Product NDC: 10019-037
Proprietary Name: Fentanyl Citrate
Non Proprietary Name: Fentanyl Citrate
Active Ingredient(s): 50    ug/mL & nbsp;   Fentanyl Citrate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl Citrate

Product NDC: 10019-037
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA019101
Marketing Category: ANDA
Start Marketing Date: 20100625

Package Information of Fentanyl Citrate

Package NDC: 10019-037-25
Package Description: 25 VIAL, SINGLE-DOSE in 1 PACKAGE (10019-037-25) > 20 mL in 1 VIAL, SINGLE-DOSE (10019-037-20)

NDC Information of Fentanyl Citrate

NDC Code 10019-037-25
Proprietary Name Fentanyl Citrate
Package Description 25 VIAL, SINGLE-DOSE in 1 PACKAGE (10019-037-25) > 20 mL in 1 VIAL, SINGLE-DOSE (10019-037-20)
Product NDC 10019-037
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fentanyl Citrate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20100625
Marketing Category Name ANDA
Labeler Name Baxter Healthcare Corporation
Substance Name FENTANYL CITRATE
Strength Number 50
Strength Unit ug/mL
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Fentanyl Citrate


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