Home Applications 019353 Application 019353
Type NDA
Sponsor AKORN Application Products# Product, Drug, Ingredient table Product Drug Ingredient Form Strength Reference drug Reference standard 001 ALFENTA ALFENTANIL HYDROCHLORIDE INJECTABLE;INJECTION EQ 0.5MG BASE/ML Yes Yes
Source provenance: Browse the complete Orange Book source catalog · source snapshot 44 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N019353-001 ALFENTA ALFENTANIL HYDROCHLORIDE EQ 0.5MG BASE/ML INJECTABLE / INJECTION RLD, RS 1986-12-29
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 2 of 2 · 44 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2022-10-28 04:53 UTC 2022-10 N019353-001 ALFENTA EQ 0.5MG BASE/ML INJECTABLE / INJECTION AP RLD, RS 1986-12-29 f41ea6bd6efb…2022-09-29 23:25 UTC 2022-09 N019353-001 ALFENTA EQ 0.5MG BASE/ML INJECTABLE / INJECTION AP RLD, RS 1986-12-29 e64feba35796…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 N019353-001 ALFENTA EQ 0.5MG BASE/ML INJECTABLE / INJECTION AP RLD, RS 1986-12-29 cb3db0bc1861…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N019353-001 ALFENTA EQ 0.5MG BASE/ML INJECTABLE / INJECTION RLD, RS 1986-12-29 a50c72e98297…
Observed Orange Book normalized TE history# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
NDC Listings For This Application# NDC listings for this application page 1 of 1 · 11 matching rows.
NDC, Name, Nonproprietary name table NDC Name Nonproprietary name Labeler Marketing category Status 17478-067 Alfentanil Hydrochloride Alfentanil Hydrochloride Akorn, Inc. NDA Current 17478-067 Alfentanil Hydrochloride Alfentanil Hydrochloride Akorn, Inc. NDA Current 17478-067 Alfentanil Hydrochloride Alfentanil Hydrochloride Akorn NDA Current 17478-067 Alfentanil Hydrochloride Alfentanil Hydrochloride Akorn NDA Current 17478-067 Alfentanil Hydrochloride Alfentanil Hydrochloride Akorn, Inc. NDA Current 17478-067 Alfentanil Hydrochloride Alfentanil Hydrochloride Akorn, Inc. NDA Current 17478-067 Alfentanil Hydrochloride Alfentanil Hydrochloride Akorn NDA Current 17478-841 Alfentanil Alfentanil Hydrochloride Akorn NDA Current 17478-841 Alfentanil Alfentanil Hydrochloride Akorn, Inc. NDA Current 17478-841 Alfentanil Alfentanil Hydrochloride Akorn, Inc. NDA Current 17478-841 Alfentanil Alfentanil Hydrochloride Akorn, Inc. NDA Current
Documents# Document, Submission type, Date table Document Submission type Date 84710 SUPPL 2026-01-07 84562 SUPPL 2025-12-29 76992 SUPPL 2023-12-19 76889 SUPPL 2023-12-18 73435 SUPPL 2023-02-09 60417 SUPPL 2019-10-09 60268 SUPPL 2019-10-07 57633 ORIG 2019-02-15 46397 SUPPL 2016-12-21 46231 SUPPL 2016-12-20 11479 SUPPL 2015-07-30 1290 SUPPL 2015-07-27