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Norepinephrine Bitartrate

NDC 51991-983, Norepinephrine Bitartrate, injection, solution, concentrate, from Breckenridge Pharmaceutical, Inc..

Product NDC
51991-983
Status
Listed
Labeler
Breckenridge Pharmaceutical, Inc.
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214455
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51991-983 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NOREPINEPHRINE BITARTRATE1 mg/mL

Pharmacologic classes

Catecholamine [EPC]; Catecholamines [CS]

Package NDCNDC-11Package
51991-983-175199109831710 VIAL, SINGLE-DOSE in 1 CARTON (51991-983-17) / 4 mL in 1 VIAL, SINGLE-DOSE (51991-983-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/109aa5e6-4e42-4131-97b0-f24d3a4cb4e8

Use it

Look up 51991-983 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51991-983 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51991-983. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.