United States · FDA National Drug Code directory
Atropine
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
- 60219-1749_1b2b68ed-bad1-4742-b88d-1d2f0040ad52
- Product NDC
- 60219-1749
- Form
- SOLUTION/ DROPS
- Composition / generic term
- atropine sulfate
- Labeler
- Amneal Pharmaceuticals NY LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220719
- Source listing expiry
- 20261231
Source-listed ingredients
- ATROPINE SULFATE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, DROPPER in 1 CARTON (60219-1749-3) / 5 mL in 1 BOTTLE, DROPPER · 60219-1749-3
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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