United States · FDA National Drug Code directory

METFORMIN HYDROCHLORIDE EXTENDED RELEASE

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
82804-148_0e1e77e6-1d37-4d24-b70d-dc2bad97b46c
Product NDC
82804-148
Form
TABLET, EXTENDED RELEASE
Composition / generic term
METFORMIN HYDROCHLORIDE
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20160512
Source listing expiry
20261231

Source-listed ingredients

  • METFORMIN HYDROCHLORIDE — 750 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-148-00) · 82804-148-00
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-148-30) · 82804-148-30

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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