Clonidine Hydrochloride
- Product NDC
- 55700-472
- 11-digit product format
- 557000472
- Labeler code
- 55700
- Product ID
- 55700-472_285f45e1-a00e-4227-a3ce-9c11d786783e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA202297
- Marketing category
- ANDA
- Marketing start
- 2013-06-17
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record