PHENYLEPHRINE HYDROCHLORIDE
NDC 70069-813, PHENYLEPHRINE HYDROCHLORIDE, injection, from Somerset Therapeutics, LLC.
- Product NDC
- 70069-813
- Status
- Listed
- Labeler
- Somerset Therapeutics, LLC
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA213318
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70069-813 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PHENYLEPHRINE HYDROCHLORIDE100 mg/10mL
Pharmacologic classes
Adrenergic alpha1-Agonists [MoA]; alpha-1 Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70069-813-01 | 70069081301 | 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (70069-813-01) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/18b65b44-fdd1-4385-b6f8-cf3cbdc8d0e6Medicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=70069-813
Use it
Look up 70069-813 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70069-813 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70069-813. 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.