Clonidine Hydrochloride
- Product NDC
- 60760-027
- 11-digit product format
- 607600027
- Labeler code
- 60760
- Product ID
- 60760-027_7a7f2f56-a679-fd89-e053-2a91aa0a4680
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St Marys Medical Park Pharmacy
- Application
- ANDA070974
- Marketing category
- ANDA
- Marketing start
- 2010-03-01
- 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