United States · FDA National Drug Code directory
ATROPINE SULFATE
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
- 51662-1289_54a277fa-4354-0791-e063-6394a90a7678
- Product NDC
- 51662-1289
- Form
- INJECTION, SOLUTION
- Composition / generic term
- ATROPINE SULFATE
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Marketing category
- NDA
- Marketing start / end (source format)
- 20180923
- Source listing expiry
- 20271231
Source-listed ingredients
- ATROPINE SULFATE — .1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 SYRINGE, PLASTIC in 1 CARTON (51662-1289-1) / 10 mL in 1 SYRINGE, PLASTIC · 51662-1289-1
- 10 POUCH in 1 CASE (51662-1289-3) / 1 CARTON in 1 POUCH (51662-1289-2) / 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC · 51662-1289-3
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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