Clonidine Hydrochloride
- Product NDC
- 0832-0777
- 11-digit product format
- 008320777
- Labeler code
- 0832
- Product ID
- 0832-0777_b6eb036e-36fd-4f4c-b57a-9a4ec6246726
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Upsher-Smith Laboratories, LLC
- Application
- ANDA211433
- Marketing category
- ANDA
- Marketing start
- 2018-10-12
- Marketing end
- 2021-06-30
- 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
- 0000-00-00
- 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 |
|---|
| 0832-0777-60 | 00832077760 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-0777-60) | 2018-10-12 | 2021-06-30 | No | No | Current |