Clonidine Hydrochloride
- Product NDC
- 71335-2889
- 11-digit product format
- 713352889
- Labeler code
- 71335
- Product ID
- 71335-2889_42540d3c-5254-6bc7-e063-6294a90adf98
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202297
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- .3 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| W76I6XXF06 | CLONIDINE HYDROCHLORIDE | 4205-91-8 | CLONIDINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2889-1 | 71335288901 | 500 TABLET in 1 BOTTLE (71335-2889-1) | 500 tablet | 2025-10-29 | No | No | Historical |