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
- 63323-751_5a89afc5-7043-4297-8f6b-f8858e9f7a83
- Product NDC
- 63323-751
- Form
- INJECTION
- Composition / generic term
- Phenylephrine Hydrochloride
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190525
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENYLEPHRINE HYDROCHLORIDE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (63323-751-05) / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE · 63323-751-05
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (63323-751-10) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE · 63323-751-10
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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