Atropine Sulfate
NDC 24208-965, Atropine Sulfate, solution, from Bausch & Lomb Incorporated.
- Product NDC
- 24208-965
- Status
- Listed
- Labeler
- Bausch & Lomb Incorporated
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA213581
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/24208-965 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ATROPINE SULFATE10 mg/mL
Pharmacologic classes
Anticholinergic [EPC]; Cholinergic Antagonists [MoA]; Cholinergic Muscarinic Antagonist [EPC]; Cholinergic Muscarinic Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 24208-965-01 | 24208096501 | 10 VIAL in 1 CARTON (24208-965-01) / .4 mL in 1 VIAL |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/aeab333c-3cdb-45c0-9e22-949624d69fbc
Use it
Look up 24208-965 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/24208-965 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 24208-965. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.