Norepinephrine Bitartrate
NDC 65219-140, NOREPINEPHRINE BITARTRATE, solution, from Fresenius Kabi USA, LLC.
- Product NDC
- 65219-140
- Status
- Listed
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211382
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/65219-140 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- NOREPINEPHRINE BITARTRATE1 mg/mL
Pharmacologic classes
Catecholamine [EPC]; Catecholamines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 65219-140-04 | 65219014004 | 10 VIAL, SINGLE-DOSE in 1 CARTON (65219-140-04) / 4 mL in 1 VIAL, SINGLE-DOSE (65219-140-02) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/dfed53ef-2060-44b8-a62e-9f8ee10a05a5
Use it
Look up 65219-140 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65219-140 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65219-140. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.