ibuprofen and famotidine

Generic: ibuprofen and famotidine

Labeler: endo usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen and famotidine
Generic Name ibuprofen and famotidine
Labeler endo usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

famotidine 26.6 mg/1, ibuprofen 800 mg/1

Manufacturer
ENDO USA, Inc.

Identifiers & Regulatory

Product NDC 49884-366
Product ID 49884-366_fc0fc3da-a5e4-4256-8b93-bf3da5bdcfc6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203658
Listing Expiration 2026-12-31
Marketing Start 2024-03-22

Pharmacologic Class

Established (EPC)
histamine-2 receptor antagonist [epc] nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
histamine h2 receptor antagonists [moa] cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49884366
Hyphenated Format 49884-366

Supplemental Identifiers

RxCUI
1100066
UPC
0349884366094
UNII
5QZO15J2Z8 WK2XYI10QM
NUI
N0000000151 N0000175784 N0000000160 M0001335 N0000175722

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ibuprofen and famotidine (source: ndc)
Generic Name ibuprofen and famotidine (source: ndc)
Application Number ANDA203658 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 26.6 mg/1
  • 800 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (49884-366-09)
source: ndc

Packages (1)

49884-366-09 90 TABLET in 1 BOTTLE (49884-366-09)

Ingredients (2)

famotidine (26.6 mg/1) ibuprofen (800 mg/1)

Linked Drug Pages (1)

Ibuprofen and famotidine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fc0fc3da-a5e4-4256-8b93-bf3da5bdcfc6", "openfda": {"nui": ["N0000000151", "N0000175784", "N0000000160", "M0001335", "N0000175722"], "upc": ["0349884366094"], "unii": ["5QZO15J2Z8", "WK2XYI10QM"], "rxcui": ["1100066"], "spl_set_id": ["b6895176-efb1-472e-8b6f-2987e8e67684"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]", "Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["ENDO USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (49884-366-09)", "package_ndc": "49884-366-09", "marketing_start_date": "20240322"}], "brand_name": "Ibuprofen and famotidine", "product_id": "49884-366_fc0fc3da-a5e4-4256-8b93-bf3da5bdcfc6", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "49884-366", "generic_name": "Ibuprofen and famotidine", "labeler_name": "ENDO USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen and famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "26.6 mg/1"}, {"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA203658", "marketing_category": "ANDA", "marketing_start_date": "20240322", "listing_expiration_date": "20261231"}