clonidine hydrochloride
- Product NDC
- 68071-4041
- 11-digit product format
- 680714041
- Labeler code
- 68071
- Product ID
- 68071-4041_d60c8b7a-7046-4b42-e053-2995a90a55ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA091368
- Marketing category
- ANDA
- Marketing start
- 2016-05-03
- 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 |
|---|
| 68071-4041-1 | 68071404101 | 100 TABLET in 1 BOTTLE (68071-4041-1) | 100 tablet | 2017-08-10 | 0000-00-00 | No | No | Current |