United States · FDA National Drug Code directory
Norepinephrine Bitartrate
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
- 71839-143_c42d425a-094e-4390-b4f9-4bb4b0fbc7d0
- Product NDC
- 71839-143
- Form
- INJECTION
- Composition / generic term
- norepinephrine bitartrate
- Labeler
- BE Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231230
- Source listing expiry
- 20261231
Source-listed ingredients
- NOREPINEPHRINE BITARTRATE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, SINGLE-DOSE in 1 CARTON (71839-143-10) / 4 mL in 1 VIAL, SINGLE-DOSE (71839-143-01) · 71839-143-10
- 25 VIAL, SINGLE-DOSE in 1 CARTON (71839-143-25) / 4 mL in 1 VIAL, SINGLE-DOSE (71839-143-01) · 71839-143-25
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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