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
- 42799-826_0e312e98-b1a3-4746-b074-b0cd28aba14e
- Product NDC
- 42799-826
- Form
- SOLUTION/ DROPS
- Composition / generic term
- Atropine sulfate
- Labeler
- Edenbridge Pharmaceuticals LLC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260506
- Source listing expiry
- 20271231
Source-listed ingredients
- ATROPINE SULFATE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (42799-826-01) / 2 mL in 1 BOTTLE · 42799-826-01
- 1 BOTTLE in 1 CARTON (42799-826-02) / 5 mL in 1 BOTTLE · 42799-826-02
- 1 BOTTLE in 1 CARTON (42799-826-03) / 15 mL in 1 BOTTLE · 42799-826-03
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →