Acamprosate Calcium
NDC 68462-435, Acamprosate Calcium, tablet, delayed release, from Glenmark Pharmaceuticals Inc., USA.
- Product NDC
- 68462-435
- Status
- Listed
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202229
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68462-435 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ACAMPROSATE CALCIUM333 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68462-435-11 | 68462043511 | 10 BLISTER PACK in 1 CARTON (68462-435-11) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
| 68462-435-18 | 68462043518 | 180 TABLET, DELAYED RELEASE in 1 BOTTLE (68462-435-18) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/43e9ef60-2d85-4394-906b-93042fea099aNADAC price for package 68462043518
GET /v1/drugs/nadac/68462043518
Use it
Look up 68462-435 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68462-435 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68462-435. 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.