Clonidine Hydrochloride
- Product NDC
- 50090-1652
- 11-digit product format
- 500901652
- Labeler code
- 50090
- Product ID
- 50090-1652_7f2a1637-265a-4146-811d-7d123b9efc30
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA070976
- Marketing category
- ANDA
- Marketing start
- 1995-01-03
- Marketing end
- 0000-00-00
- Substance
- CLONIDINE HYDRO
- Active strength
- 0 mg/1
- Pharmacologic classes
- Adrenergic alph
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record