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Fentanyl Citrate - 0641-6027-25 - (Fentanyl Citrate)

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Drug Information of Fentanyl Citrate

Product NDC: 0641-6027
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
Coding System: National Drug Codes(NDC)

Labeler Information of Fentanyl Citrate

Product NDC: 0641-6027
Labeler Name: West-ward Pharmaceutical Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA019101
Marketing Category: ANDA
Start Marketing Date: 19840711

Package Information of Fentanyl Citrate

Package NDC: 0641-6027-25
Package Description: 25 VIAL in 1 CARTON (0641-6027-25) > 2 mL in 1 VIAL (0641-6027-01)

NDC Information of Fentanyl Citrate

NDC Code 0641-6027-25
Proprietary Name Fentanyl Citrate
Package Description 25 VIAL in 1 CARTON (0641-6027-25) > 2 mL in 1 VIAL (0641-6027-01)
Product NDC 0641-6027
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fentanyl Citrate
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19840711
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp.
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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