Clonidine hydrochloride
NDC 68001-568, Clonidine hydrochloride, tablet, extended release, from BluePoint Laboratories.
- Product NDC
- 68001-568
- Status
- Listed
- Labeler
- BluePoint Laboratories
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209686
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68001-568 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CLONIDINE HYDROCHLORIDE.1 mg/1
Pharmacologic classes
Adrenergic alpha2-Agonists [MoA]; Central alpha-2 Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68001-568-06 | 68001056806 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-568-06) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/f34ae077-4ace-4e0a-bc87-d559b1c5bf2fNADAC price for package 68001056806
GET /v1/drugs/nadac/68001056806
Use it
Look up 68001-568 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68001-568 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68001-568. 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.