Clonidine Hydrochloride
- Product NDC
- 10370-302
- 11-digit product format
- 103700302
- Labeler code
- 10370
- Product ID
- 10370-302_97fe07e4-729a-4538-a6be-adee45d97596
- 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
- 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
- 2020-12-31
- 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 |
|---|
| 10370-302-02 | 10370030202 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (10370-302-02) | 2013-09-30 | 0000-00-00 | No | No | Current |
| 10370-302-05 | 10370030205 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (10370-302-05) | 2013-09-30 | 0000-00-00 | No | No | Current |
| 10370-302-13 | 10370030213 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (10370-302-13) | 2013-09-30 | 0000-00-00 | No | No | Current |