Prochlorperazine Edisylate
NDC 68083-436, Prochlorperazine Edisylate, injection, from Gland Pharma Limited.
- Product NDC
- 68083-436
- Status
- Listed
- Labeler
- Gland Pharma Limited
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR, INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA214107
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68083-436 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PROCHLORPERAZINE EDISYLATE5 mg/mL
Pharmacologic classes
Phenothiazine [EPC]; Phenothiazines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68083-436-01 | 68083043601 | 1 VIAL in 1 CARTON (68083-436-01) / 10 mL in 1 VIAL |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/a0fd3d58-7470-4d0f-9e6c-84e92c02a97f
Use it
Look up 68083-436 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68083-436 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68083-436. 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.