Clonidine Hydrochloride
- Product NDC
- 68788-7685
- 11-digit product format
- 687887685
- Labeler code
- 68788
- Product ID
- 68788-7685_e706e15e-b0ae-4af3-962b-4d200cf6e1dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA070975
- Marketing category
- ANDA
- Marketing start
- 2020-04-01
- 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 |
|---|
| 68788-7685-3 | 68788768503 | 30 TABLET in 1 BOTTLE (68788-7685-3) | 30 tablet | 2020-04-01 | 0000-00-00 | No | No | Current |
| 68788-7685-6 | 68788768506 | 60 TABLET in 1 BOTTLE (68788-7685-6) | 60 tablet | 2020-04-01 | 0000-00-00 | No | No | Current |
| 68788-7685-9 | 68788768509 | 90 TABLET in 1 BOTTLE (68788-7685-9) | 90 tablet | 2020-04-01 | 0000-00-00 | No | No | Current |