United States · FDA National Drug Code directory
Biorphen
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
- 43598-172_884b0378-92e0-f3ed-176b-ff409f29747f
- Product NDC
- 43598-172
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Phenylephrine hydrochloride
- Labeler
- Dr. Reddy's Laboratories Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20221125
- Source listing expiry
- 20271231
Source-listed ingredients
- PHENYLEPHRINE HYDROCHLORIDE — .1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 AMPULE in 1 CARTON (43598-172-15) / 5 mL in 1 AMPULE (43598-172-05) · 43598-172-15
- 5 mL in 1 VIAL (43598-172-25) · 43598-172-25
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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