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Medicines · US (FDA)

FDA 2011

FDA

Fentanyl Citrate

Approved 7 Jan 2011Buccal, Under the tongueTablet

The FDA lists this product in 38 strengths and forms.

Official labelAsk Osler about it

On this page

Composition
Strengths and forms
Official product information

The table holds no label text for this product yet, only the facts beside it. The official product information has the full text.

Composition

Active ingredients: FENTANYL CITRATE EQ 0.6MG BASE

Strengths and forms

The FDA lists each strength of a product separately; these pages share one label.

FENTANYL CITRATE EQ 0.6MG BASE · Troche/lozengeANDA077312-003 · Discontinued
FENTANYL CITRATE EQ 0.2MG BASE · Troche/lozengeANDA077312-001 · Discontinued
FENTANYL CITRATE EQ 1.6MG BASE · Troche/lozengeANDA077312-006 · Discontinued
FENTANYL CITRATE EQ 0.8MG BASE · Troche/lozengeANDA077312-004 · Discontinued
FENTANYL CITRATE EQ 0.4MG BASE · Troche/lozengeANDA077312-002 · Discontinued
FENTANYL CITRATE EQ 1.2MG BASE · Troche/lozengeANDA077312-005 · Discontinued
FENTANYL CITRATE EQ 0.6MG BASE · Troche/lozengeANDA078907-003 · Discontinued
FENTANYL CITRATE EQ 0.2MG BASE · Troche/lozengeANDA078907-001 · Discontinued
FENTANYL CITRATE EQ 1.6MG BASE · Troche/lozengeANDA078907-006 · Discontinued
FENTANYL CITRATE EQ 0.8MG BASE · Troche/lozengeANDA078907-004 · Discontinued
FENTANYL CITRATE EQ 0.4MG BASE · Troche/lozengeANDA078907-002 · Discontinued

At a glance

Brand name: Fentanyl Citrate
Route: Buccal, Under the tongue
Dosage form: Tablet
Applicant: Watson Labs
Status: Discontinued
FDA approval: 7 Jan 2011
Application: ANDA079075-004

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

FENTANYL CITRATE EQ 1.2MG BASE · Troche/lozengeANDA078907-005 · Discontinued

FENTANYL CITRATE EQ 0.05MG BASE/ML · InjectableNDA019115-001 · Prescription

FENTANYL CITRATE EQ 2.5MG BASE/50ML (EQ 0.05MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · SolutionNDA215870-001 · Discontinued

FENTANYL CITRATE EQ 5MG BASE/100ML (EQ 0.05MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · SolutionNDA215870-002 · Discontinued

FENTANYL CITRATE EQ 0.05MG BASE/ML · InjectableANDA212086-001 · Prescription

FENTANYL CITRATE EQ 0.05MG BASE/ML · InjectableANDA073488-001 · Discontinued

FENTANYL CITRATE EQ 0.6MG BASE · TabletThis page

FENTANYL CITRATE EQ 0.2MG BASE · TabletANDA079075-002 · Discontinued

FENTANYL CITRATE EQ 0.8MG BASE · TabletANDA079075-005 · Discontinued

FENTANYL CITRATE EQ 0.4MG BASE · TabletANDA079075-003 · Discontinued

FENTANYL CITRATE EQ 0.1MG BASE · TabletANDA079075-001 · Discontinued

FENTANYL CITRATE EQ 0.8MG BASE · TabletANDA206329-006 · Discontinued

FENTANYL CITRATE EQ 0.4MG BASE · TabletANDA206329-004 · Discontinued

FENTANYL CITRATE EQ 0.2MG BASE · TabletANDA206329-002 · Discontinued

FENTANYL CITRATE EQ 0.6MG BASE · TabletANDA206329-005 · Discontinued

FENTANYL CITRATE EQ 0.3MG BASE · TabletANDA206329-003 · Discontinued

FENTANYL CITRATE EQ 0.1MG BASE · TabletANDA206329-001 · Discontinued

FENTANYL CITRATE EQ 0.05MG BASE/ML · InjectableANDA070636-001 · Discontinued

FENTANYL CITRATE EQ 0.05MG BASE/ML · InjectableANDA070637-001 · Discontinued

FENTANYL CITRATE EQ 0.025MG BASE/0.5ML · InjectableNDA019101-002 · Prescription

FENTANYL CITRATE EQ 0.05MG BASE/ML · InjectableNDA019101-001 · Prescription

FENTANYL CITRATE EQ 0.8MG BASE · TabletANDA207338-006 · Discontinued

FENTANYL CITRATE EQ 0.4MG BASE · TabletANDA207338-004 · Discontinued

FENTANYL CITRATE EQ 0.2MG BASE · TabletANDA207338-002 · Discontinued

FENTANYL CITRATE EQ 0.6MG BASE · TabletANDA207338-005 · Discontinued

FENTANYL CITRATE EQ 0.3MG BASE · TabletANDA207338-003 · Discontinued

FENTANYL CITRATE EQ 0.1MG BASE · TabletANDA207338-001 · Discontinued

Official product information

Drugs@FDA lists the approved labels, letters and reviews for application ANDA079075.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.