Clonidine Hydrochloride
- Product NDC
- 50090-0135
- 11-digit product format
- 500900135
- Labeler code
- 50090
- Product ID
- 50090-0135_da1aee4d-c5fc-45bd-a07a-4ce79ccbbb3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record