Clonidine Hydrochloride
- Product NDC
- 10370-257
- 11-digit product format
- 103700257
- Labeler code
- 10370
- Product ID
- 10370-257_b0fc36fe-3c35-413c-abbe-106aea5b08bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA202984
- Marketing category
- ANDA
- Marketing start
- 2013-09-30
- Marketing end
- 2023-04-30
- 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 |
|---|
| 10370-257-02 | 10370025702 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (10370-257-02) | 2013-09-30 | 0000-00-00 | No | No | Current |
| 10370-257-05 | 10370025705 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (10370-257-05) | 2013-09-30 | 0000-00-00 | No | No | Current |
| 10370-257-13 | 10370025713 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (10370-257-13) | 2013-09-30 | 0000-00-00 | No | No | Current |