United States · FDA National Drug Code directory

Children Allergy

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
37808-654_24026246-18c5-41b2-b760-b2552505292e
Product NDC
37808-654
Form
SUSPENSION
Composition / generic term
Fexofenadine HCL
Labeler
H E B
Marketing category
ANDA
Marketing start / end (source format)
20231031 / 20261228

Source-listed ingredients

  • FEXOFENADINE HYDROCHLORIDE — 30 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, PLASTIC in 1 BOX (37808-654-04) / 118 mL in 1 BOTTLE, PLASTIC · 37808-654-04

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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