Clonidine Hydrochloride
- Product NDC
- 63629-9289
- 11-digit product format
- 636299289
- Labeler code
- 63629
- Product ID
- 63629-9289_a417b52d-bd77-41a3-8d8b-359cfa62a6e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202297
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-9289-1 | 63629928901 | 100 TABLET in 1 BOTTLE (63629-9289-1) | 100 tablet | 2022-06-06 | 0000-00-00 | No | No | Current |