Home Applications 201272 Application 201272
Type ANDA
Sponsor INTELLIPHARMACEUTICS Application Products# Product, Drug, Ingredient table Product Drug Ingredient Form Strength Reference drug Reference standard 001 VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 37.5MG BASE No No 002 VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 75MG BASE No No 003 VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL EQ 150MG BASE No No
Source provenance: Browse the complete Orange Book source catalog · source snapshot 44 .
Orange Book products# Current product rows page 1 of 1 · 3 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A201272-001 VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE EQ 37.5MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 A201272-002 VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE EQ 75MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 A201272-003 VENLAFAXINE HYDROCHLORIDE VENLAFAXINE HYDROCHLORIDE EQ 150MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 3 matching rows.
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 4 of 4 · 132 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 A201272-001 VENLAFAXINE HYDROCHLORIDE EQ 37.5MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 f41ea6bd6efb…2022-10-28 04:53 UTC 2022-10 A201272-002 VENLAFAXINE HYDROCHLORIDE EQ 75MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 f41ea6bd6efb…2022-10-28 04:53 UTC 2022-10 A201272-003 VENLAFAXINE HYDROCHLORIDE EQ 150MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 f41ea6bd6efb…2022-09-29 23:25 UTC 2022-09 A201272-001 VENLAFAXINE HYDROCHLORIDE EQ 37.5MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 e64feba35796…2022-09-29 23:25 UTC 2022-09 A201272-002 VENLAFAXINE HYDROCHLORIDE EQ 75MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 e64feba35796…2022-09-29 23:25 UTC 2022-09 A201272-003 VENLAFAXINE HYDROCHLORIDE EQ 150MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 e64feba35796…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A201272-001 VENLAFAXINE HYDROCHLORIDE EQ 37.5MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 cb3db0bc1861…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A201272-002 VENLAFAXINE HYDROCHLORIDE EQ 75MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 cb3db0bc1861…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A201272-003 VENLAFAXINE HYDROCHLORIDE EQ 150MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 cb3db0bc1861…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A201272-001 VENLAFAXINE HYDROCHLORIDE EQ 37.5MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A201272-002 VENLAFAXINE HYDROCHLORIDE EQ 75MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A201272-003 VENLAFAXINE HYDROCHLORIDE EQ 150MG BASE CAPSULE, EXTENDED RELEASE / ORAL AB 2018-11-23 a50c72e98297…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 4 · 132 observed states.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
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 · 3 matching rows.
NDC, Name, Nonproprietary name table NDC Name Nonproprietary name Labeler Marketing category Status 35208-011 Venlafaxine Hydrochloride Venlafaxine Hydrochloride IntelliPharmaCeutics Corp. ANDA Current 35208-012 Venlafaxine Hydrochloride Venlafaxine Hydrochloride IntelliPharmaCeutics Corp. ANDA Current 35208-013 Venlafaxine Hydrochloride Venlafaxine Hydrochloride IntelliPharmaCeutics Corp. ANDA Current