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
- 51991-983_e78a060d-1195-4127-95ca-08f3fee36c43
- Product NDC
- 51991-983
- Form
- INJECTION, SOLUTION, CONCENTRATE
- Composition / generic term
- Norepinephrine Bitartrate
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210701
- Source listing expiry
- 20271231
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 (51991-983-17) / 4 mL in 1 VIAL, SINGLE-DOSE (51991-983-99) · 51991-983-17
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 →