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
- 70512-866_45728b25-194d-ddeb-e063-6294a90af4c9
- Product NDC
- 70512-866
- Form
- SOLUTION/ DROPS
- Composition / generic term
- Phenylephrine Hydrochloride
- Labeler
- SOLA Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240601
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENYLEPHRINE HYDROCHLORIDE — 100 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, DROPPER in 1 CARTON (70512-866-05) / 5 mL in 1 BOTTLE, DROPPER · 70512-866-05
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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