clonidine hydrochloride
- Product NDC
- 68788-7380
- 11-digit product format
- 687887380
- Labeler code
- 68788
- Product ID
- 68788-7380_11c93e4a-0996-4557-9ee5-9769604d0640
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078895
- Marketing category
- ANDA
- Marketing start
- 2016-08-31
- 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 |
|---|
| 68788-7380-3 | 68788738003 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-7380-3) | 30 tablet | 2016-08-31 | 0000-00-00 | No | No | Current |
| 68788-7380-6 | 68788738006 | 60 TABLET in 1 BOTTLE, PLASTIC (68788-7380-6) | 60 tablet | 2016-08-31 | 0000-00-00 | No | No | Current |
| 68788-7380-9 | 68788738009 | 90 TABLET in 1 BOTTLE, PLASTIC (68788-7380-9) | 90 tablet | 2016-08-31 | 0000-00-00 | No | No | Current |