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
- 68083-669_01f9b403-5ef9-4364-9138-7e7f65248bde
- Product NDC
- 68083-669
- Form
- SOLUTION/ DROPS
- Composition / generic term
- Atropine Sulfate
- Labeler
- Gland Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260731
- 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, DROPPER in 1 CARTON (68083-669-01) / 2 mL in 1 BOTTLE, DROPPER · 68083-669-01
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 →