allergy relief

Generic: fexofenadine hydrochloride

Labeler: aaa pharmaceutical, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name fexofenadine hydrochloride
Labeler aaa pharmaceutical, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fexofenadine hydrochloride 180 mg/1

Manufacturer
AAA PHARMACEUTICAL, INC.

Identifiers & Regulatory

Product NDC 57344-292
Product ID 57344-292_1e038697-ba15-dca2-e063-6394a90a0bee
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211075
Listing Expiration 2026-12-31
Marketing Start 2021-07-06

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 57344292
Hyphenated Format 57344-292

Supplemental Identifiers

RxCUI
997420
UNII
2S068B75ZU

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 allergy relief (source: ndc)
Generic Name fexofenadine hydrochloride (source: ndc)
Application Number ANDA211075 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (57344-292-02) / 5 TABLET in 1 BLISTER PACK
  • 1 BLISTER PACK in 1 CARTON (57344-292-03) / 5 TABLET in 1 BLISTER PACK
  • 1 BOTTLE, PLASTIC in 1 CARTON (57344-292-04) / 30 TABLET in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (57344-292-06) / 45 TABLET in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (57344-292-17) / 30 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (5)

57344-292-02 1 BLISTER PACK in 1 CARTON (57344-292-02) / 5 TABLET in 1 BLISTER PACK 57344-292-03 1 BLISTER PACK in 1 CARTON (57344-292-03) / 5 TABLET in 1 BLISTER PACK 57344-292-04 1 BOTTLE, PLASTIC in 1 CARTON (57344-292-04) / 30 TABLET in 1 BOTTLE, PLASTIC 57344-292-06 1 BOTTLE, PLASTIC in 1 CARTON (57344-292-06) / 45 TABLET in 1 BOTTLE, PLASTIC 57344-292-17 1 BOTTLE, PLASTIC in 1 CARTON (57344-292-17) / 30 TABLET in 1 BOTTLE, PLASTIC

Ingredients (1)

fexofenadine hydrochloride (180 mg/1)

Linked Drug Pages (1)

Allergy Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1e038697-ba15-dca2-e063-6394a90a0bee", "openfda": {"unii": ["2S068B75ZU"], "rxcui": ["997420"], "spl_set_id": ["c547c163-2a19-10d8-e053-2a95a90ac817"], "manufacturer_name": ["AAA PHARMACEUTICAL, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (57344-292-02)  / 5 TABLET in 1 BLISTER PACK", "package_ndc": "57344-292-02", "marketing_start_date": "20210706"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (57344-292-03)  / 5 TABLET in 1 BLISTER PACK", "package_ndc": "57344-292-03", "marketing_start_date": "20210706"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (57344-292-04)  / 30 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "57344-292-04", "marketing_start_date": "20210706"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (57344-292-06)  / 45 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "57344-292-06", "marketing_start_date": "20210706"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (57344-292-17)  / 30 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "57344-292-17", "marketing_start_date": "20240724"}], "brand_name": "Allergy Relief", "product_id": "57344-292_1e038697-ba15-dca2-e063-6394a90a0bee", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "57344-292", "generic_name": "Fexofenadine Hydrochloride", "labeler_name": "AAA PHARMACEUTICAL, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA211075", "marketing_category": "ANDA", "marketing_start_date": "20210706", "listing_expiration_date": "20261231"}