Package 43598-892-00

Generic: fexofenadine hcl and pseudoephedrine hcl
NDC Package

Package Facts

Identity

Package NDC 43598-892-00
Digits Only 4359889200
Product NDC 43598-892
Product ID 43598-892_e12efd76-47f6-fba9-5aad-5230c1a9f542
Description

50000 TABLET, EXTENDED RELEASE in 1 DRUM (43598-892-00)

Marketing

Marketing Status
Discontinued 2026-08-31
Generic fexofenadine hcl and pseudoephedrine hcl

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "e12efd76-47f6-fba9-5aad-5230c1a9f542", "openfda": {}, "finished": false, "packaging": [{"description": "50000 TABLET, EXTENDED RELEASE in 1 DRUM (43598-892-00)", "package_ndc": "43598-892-00", "marketing_end_date": "31-AUG-26", "marketing_start_date": "17-MAY-22"}], "product_id": "43598-892_e12efd76-47f6-fba9-5aad-5230c1a9f542", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "43598-892", "generic_name": "Fexofenadine HCl and Pseudoephedrine HCl", "labeler_name": "Dr.Reddy's Laboratories Inc", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "240 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_end_date": "20260831", "marketing_start_date": "20220517"}