United States · FDA National Drug Code directory
phenylephrine hydrochloride
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
- 36000-362_74192a42-0ff7-443b-9d8a-3096ef5c8e43
- Product NDC
- 36000-362
- Form
- INJECTION
- Composition / generic term
- phenylephrine hydrochloride
- Labeler
- Baxter Healthcare Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260406
- Source listing expiry
- 20271231
Source-listed ingredients
- PHENYLEPHRINE HYDROCHLORIDE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (36000-362-05) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE · 36000-362-05
Source and coverage
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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.
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