Clonidine Hydrochloride
- Product NDC
- 0904-5657
- 11-digit product format
- 009045657
- Labeler code
- 0904
- Product ID
- 0904-5657_52005146-b3aa-4eb5-ac04-f796924b0104
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA070975
- Marketing category
- ANDA
- Marketing start
- 2006-11-20
- 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