Prochlorperazine Maleate
NDC 70771-1697, Prochlorperazine Maleate, tablet, from Zydus Lifesciences Limited.
- Product NDC
- 70771-1697
- Status
- Listed
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA216495
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1697 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PROCHLORPERAZINE MALEATE5 mg/1
Pharmacologic classes
Phenothiazine [EPC]; Phenothiazines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70771-1697-1 | 70771169701 | 100 TABLET in 1 BOTTLE (70771-1697-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/1e7fd1f5-c9cc-45a2-8974-4e0ceab8406c
Use it
Look up 70771-1697 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1697 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70771-1697. 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.