Clonidine hydrochloride
- Product NDC
- 71205-829
- 11-digit product format
- 712050829
- Labeler code
- 71205
- Product ID
- 71205-829_8427eee0-955d-4718-b259-73dab56d36d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA070924
- Marketing category
- ANDA
- Marketing start
- 2017-06-01
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- .2 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 |
|---|
| 71205-829-30 | 71205082930 | 30 TABLET in 1 BOTTLE (71205-829-30) | 30 tablet | 2023-08-18 | No | No | Historical |
| 71205-829-60 | 71205082960 | 60 TABLET in 1 BOTTLE (71205-829-60) | 60 tablet | 2023-08-18 | No | No | Historical |
| 71205-829-90 | 71205082990 | 90 TABLET in 1 BOTTLE (71205-829-90) | 90 tablet | 2023-08-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Clonidine hydrochloride | Proficient Rx LP | 2023-08-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |