Home NDC 70771-1924 Ibuprofen and Famotidine
Product NDC 70771-1924
11-digit product format 707711924
Labeler code 70771
Product ID 70771-1924_099f42a7-f7c9-49f0-8b83-74670cc8124a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Ibuprofen and Famotidine
Dosage form TABLET
Route ORAL
Labeler Zydus Lifesciences Limited
Application ANDA218684
Marketing category ANDA
Marketing start 2025-06-01
Substance IBUPROFEN; FAMOTIDINE
Active strength 800; 26.6 mg/1; mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing 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 A218684-001 IBUPROFEN AND FAMOTIDINE FAMOTIDINE; IBUPROFEN 26.6MG;800MG TABLET / ORAL AB 2025-02-20
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code A218684-001 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 2026-10-15 13:18:30 2026-09 A218684-001 IBUPROFEN AND FAMOTIDINE 26.6MG;800MG TABLET / ORAL AB 2025-02-20 c2088c7a36db…2026-09-14 22:38:34 2026-08 A218684-001 IBUPROFEN AND FAMOTIDINE 26.6MG;800MG TABLET / ORAL AB 2025-02-20 84e616aacf4f…2026-08-18 06:07:40 2026-07 A218684-001 IBUPROFEN AND FAMOTIDINE 26.6MG;800MG TABLET / ORAL AB 2025-02-20 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A218684-001 IBUPROFEN AND FAMOTIDINE 26.6MG;800MG TABLET / ORAL AB 2025-02-20 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A218684-001 IBUPROFEN AND FAMOTIDINE 26.6MG;800MG TABLET / ORAL AB 2025-02-20 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A218684-001 IBUPROFEN AND FAMOTIDINE 26.6MG;800MG TABLET / ORAL AB 2025-02-20 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A218684-001 IBUPROFEN AND FAMOTIDINE 26.6MG;800MG TABLET / ORAL AB 2025-02-20 fd3edfee7708…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A218684-001 IBUPROFEN AND FAMOTIDINE 26.6MG;800MG TABLET / ORAL AB 2025-02-20 a50c72e98297…
Observed Orange Book normalized TE history# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Ibuprofen and Famotidine
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength IBUPROFEN 800 mg/1 FAMOTIDINE 26.6 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination WK2XYI10QM Internal UNII lookup 5QZO15J2Z8 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1100066 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70771-1924-9 Ibuprofen and Famotidine 90 in 1 BOTTLE TABLET 90 1
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 · 4 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 70771-1924-9 70771192409 90 TABLET in 1 BOTTLE (70771-1924-9) 90 tablet 2025-06-01 No No Current