Clonidine Hydrochloride
- Product NDC
- 0904-5656
- 11-digit product format
- 009045656
- Labeler code
- 0904
- Product ID
- 0904-5656_e6c8545d-096f-47b8-bf52-caba27616ea8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA070974
- Marketing category
- ANDA
- Marketing start
- 2006-11-20
- Marketing end
- 2021-03-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-5656-61 | 00904565661 | 100 BLISTER PACK in 1 CARTON (0904-5656-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2006-11-20 | 2021-03-31 | No | No | Current |