clonidine hydrochloride
- Product NDC
- 68788-7261
- 11-digit product format
- 687887261
- Labeler code
- 68788
- Product ID
- 68788-7261_9aa28816-0313-4306-8767-afee4dbef7c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA091368
- Marketing category
- ANDA
- Marketing start
- 2018-09-24
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7261-3 | 68788726103 | 30 TABLET in 1 BOTTLE (68788-7261-3) | 30 tablet | 2018-09-24 | 0000-00-00 | No | No | Current |
| 68788-7261-6 | 68788726106 | 60 TABLET in 1 BOTTLE (68788-7261-6) | 60 tablet | 2018-09-24 | 0000-00-00 | No | No | Current |
| 68788-7261-9 | 68788726109 | 90 TABLET in 1 BOTTLE (68788-7261-9) | 90 tablet | 2018-09-24 | 0000-00-00 | No | No | Current |