clonidine hydrochloride
- Product NDC
- 51862-060
- 11-digit product format
- 518620060
- Labeler code
- 51862
- Product ID
- 51862-060_8638f327-115f-452d-acbf-0924d5c65c63
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Mayne Pharma Inc.
- Application
- ANDA210680
- Marketing category
- ANDA
- Marketing start
- 2018-06-27
- Marketing end
- 0000-00-00
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51862-060-60 | 51862006060 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (51862-060-60) | 2018-06-27 | 0000-00-00 | No | No | Current |