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
- 70121-1706_cd6e7dcc-16d0-4663-859e-c22fe300a536
- Product NDC
- 70121-1706
- Form
- INJECTION, SOLUTION
- Composition / generic term
- atropine sulfate
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240109
- Source listing expiry
- 20261231
Source-listed ingredients
- ATROPINE SULFATE — .1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TRAY in 1 CARTON (70121-1706-2) / 5 SYRINGE, GLASS in 1 TRAY / 10 mL in 1 SYRINGE, GLASS · 70121-1706-2
- 24 CARTON in 1 PACKAGE (70121-1706-4) / 1 SYRINGE, GLASS in 1 CARTON (70121-1706-1) / 10 mL in 1 SYRINGE, GLASS · 70121-1706-4
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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