United States · FDA National Drug Code directory

Hydrochlorothiazide

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
50268-404_47e556aa-a6c4-b2a6-e063-6294a90ac94a
Product NDC
50268-404
Form
CAPSULE
Composition / generic term
Hydrochlorothiazide
Labeler
AvPAK
Marketing category
ANDA
Marketing start / end (source format)
20221208
Source listing expiry
20271231

Source-listed ingredients

  • HYDROCHLOROTHIAZIDE — 12.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 50 BLISTER PACK in 1 BOX (50268-404-15) / 1 CAPSULE in 1 BLISTER PACK (50268-404-11) · 50268-404-15

Source and coverage

Open FDA National Drug Code directory

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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