Clonidine Hydrochloride
- Product NDC
- 55154-7997
- 11-digit product format
- 551547997
- Labeler code
- 55154
- Product ID
- 55154-7997_b2606aa5-cae8-4c3c-9ce5-c6adae184096
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA070975
- Marketing category
- ANDA
- Marketing start
- 2006-11-20
- Marketing end
- 2021-06-30
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-7997-0 | 55154799700 | 10 BLISTER PACK in 1 BAG (55154-7997-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2006-11-20 | 2021-06-30 | No | No | Current |