Clonidine Hydrochloride
- Product NDC
- 71335-9682
- 11-digit product format
- 713359682
- Labeler code
- 71335
- Product ID
- 71335-9682_652ef659-0000-41d2-8fdb-b4dcd4105c17
- 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 |
|---|
| 71335-9682-1 | 71335968201 | 60 TABLET in 1 BOTTLE (71335-9682-1) | 60 tablet | 2024-04-03 | No | No | Historical |
| 71335-9682-2 | 71335968202 | 30 TABLET in 1 BOTTLE (71335-9682-2) | 30 tablet | 2024-04-03 | No | No | Historical |
| 71335-9682-3 | 71335968203 | 90 TABLET in 1 BOTTLE (71335-9682-3) | 90 tablet | 2024-04-03 | No | No | Historical |
| 71335-9682-4 | 71335968204 | 120 TABLET in 1 BOTTLE (71335-9682-4) | 120 tablet | 2024-04-03 | No | No | Historical |