Citalopram Hydrobromide
NDC 65862-074, Citalopram Hydrobromide, solution, from Aurobindo Pharma Limited.
- Product NDC
- 65862-074
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077812
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/65862-074 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CITALOPRAM HYDROBROMIDE10 mg/5mL
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC]; Serotonin Uptake Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 65862-074-24 | 65862007424 | 240 mL in 1 BOTTLE (65862-074-24) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e7a2cbdd-1bdb-4e59-a3dd-298a189753ae
Use it
Look up 65862-074 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65862-074 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65862-074. 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.