Clonidine Hydrochloride
- Product NDC
- 63629-8044
- 11-digit product format
- 636298044
- Labeler code
- 63629
- Product ID
- 63629-8044_0d1985dc-ee73-4387-901f-310de2d3c17f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA070974
- Marketing category
- ANDA
- Marketing start
- 1995-01-03
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63629-8044-1 | 63629804401 | 60 TABLET in 1 BOTTLE (63629-8044-1) | 60 tablet | 2019-07-18 | 0000-00-00 | No | No | Current |
| 63629-8044-2 | 63629804402 | 30 TABLET in 1 BOTTLE (63629-8044-2) | 30 tablet | 2019-07-18 | 0000-00-00 | No | No | Current |