United States · FDA National Drug Code directory

Ertapenem

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
72266-159_181c0b9d-794e-3e8a-e063-6394a90a7f16
Product NDC
72266-159
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
Ertapenem Sodium
Labeler
Fosun Pharma USA Inc
Marketing category
ANDA
Marketing start / end (source format)
20211101
Source listing expiry
20261231

Source-listed ingredients

  • ERTAPENEM SODIUM — 1 g/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 5 VIAL, SINGLE-DOSE in 1 CARTON (72266-159-05) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (72266-159-01) · 72266-159-05
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (72266-159-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (72266-159-01) · 72266-159-10

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.

Browse United States records →