Phenylephrine Hydrochloride
NDC 65219-388, Phenylephrine Hydrochloride, injection, from Fresenius Kabi USA, LLC.
- Product NDC
- 65219-388
- Status
- Listed
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210665
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/65219-388 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PHENYLEPHRINE HYDROCHLORIDE10 mg/mL
Pharmacologic classes
Adrenergic alpha1-Agonists [MoA]; alpha-1 Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 65219-388-01 | 65219038801 | 25 VIAL, SINGLE-DOSE in 1 CARTON (65219-388-01) / 1 mL in 1 VIAL, SINGLE-DOSE (65219-388-00) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/b54a0c59-e5e4-4fd7-ba91-c991ce87b148
Use it
Look up 65219-388 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65219-388 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65219-388. 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.