Clonidine Hydrochloride
- Product NDC
- 70518-2110
- 11-digit product format
- 705182110
- Labeler code
- 70518
- Product ID
- 70518-2110_8995a9b1-9f96-0e78-e053-2995a90a0e07
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209285
- Marketing category
- ANDA
- Marketing start
- 2019-05-23
- 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