clonidine hydrochloride
- Product NDC
- 68071-4082
- 11-digit product format
- 680714082
- Labeler code
- 68071
- Product ID
- 68071-4082_588a62df-3e5b-15c2-e053-2991aa0a30bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA091368
- Marketing category
- ANDA
- Marketing start
- 2016-05-03
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record