Clonidine Hydrochloride
- Product NDC
- 68788-9213
- 11-digit product format
- 687889213
- Labeler code
- 68788
- Product ID
- 68788-9213_edcf576a-29e0-41fe-96f5-dbd8c8546b64
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA070975
- Marketing category
- ANDA
- Marketing start
- 2011-11-10
- 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