United States · FDA National Drug Code directory

Metformin Hydrochloride

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
50090-5396_060b6bdc-9ddc-4a8f-9c90-d686707bc9ce
Product NDC
50090-5396
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Metformin Hydrochloride
Labeler
A-S Medication Solutions
Marketing category
ANDA
Marketing start / end (source format)
20181027
Source listing expiry
20261231

Source-listed ingredients

  • METFORMIN HYDROCHLORIDE — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5396-0) · 50090-5396-0
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5396-1) · 50090-5396-1
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5396-2) · 50090-5396-2
  • 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5396-3) · 50090-5396-3
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5396-4) · 50090-5396-4

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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