pantoprazole sodium
NDC 70010-190, pantoprazole sodium, tablet, delayed release, from Granules Pharmaceuticals Inc..
- Product NDC
- 70010-190
- Status
- Listed
- Labeler
- Granules Pharmaceuticals Inc.
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217282
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70010-190 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PANTOPRAZOLE SODIUM20 mg/1
Pharmacologic classes
Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70010-190-09 | 70010019009 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-190-09) |
| 70010-190-10 | 70010019010 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-190-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/8f2fb647-15bc-41cb-84a4-02e956e614fcNADAC price for package 70010019009
GET /v1/drugs/nadac/70010019009
Use it
Look up 70010-190 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70010-190 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70010-190. 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.