Clonidine Hydrochloride
- Product NDC
- 0378-0152
- 11-digit product format
- 003780152
- Labeler code
- 0378
- Product ID
- 0378-0152_c16087c0-cf3a-46c3-8151-81895c298888
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA070317
- Marketing category
- ANDA
- Marketing start
- 1987-06-09
- Marketing end
- 2020-09-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record