Home Applications 217330 Application 217330
Type ANDA
Sponsor ANNORA PHARMA Application Products# Product, Drug, Ingredient table Product Drug Ingredient Form Strength Reference drug Reference standard 001 FAMOTIDINE FAMOTIDINE FOR SUSPENSION;ORAL 40MG/5ML No No
Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
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 A217330-001 FAMOTIDINE FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code A217330-001 AB
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.
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 2026-02-19 14:30 UTC 2026-02 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 8072bd15b7f6…2024-03-16 18:09 UTC · 4 captures of this ZIP 2024-03 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 6a51e52b5d6a…2024-02-18 07:12 UTC 2024-02 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 1c564ffb4f44…2023-12-20 04:57 UTC 2023-12 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 ea1830bbd6c7…2023-11-28 05:40 UTC · 2 captures of this ZIP 2023-11 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 a72a2bbeb626…2023-10-25 00:34 UTC · 2 captures of this ZIP 2023-10 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 9b2671bbb829…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A217330-001 FAMOTIDINE 40MG/5ML FOR SUSPENSION / ORAL AB 2023-08-17 a50c72e98297…
Observed Orange Book normalized TE history# 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.