clonidine hydrochloride
- Product NDC
- 16714-839
- 11-digit product format
- 167140839
- Labeler code
- 16714
- Product ID
- 16714-839_bc335d68-981c-46c3-8f01-604fe62d54ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA210680
- Marketing category
- ANDA
- Marketing start
- 2018-06-18
- 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 |
|---|
| 16714-839-01 | 16714083901 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-839-01) | 2018-06-18 | 0000-00-00 | No | No | Current |