Clonidine Hydrochloride
- Product NDC
- 72162-1679
- 11-digit product format
- 721621679
- Labeler code
- 72162
- Product ID
- 72162-1679_e374ef7b-3419-46b3-8fb0-21beeb345861
- 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
- .1 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 |
|---|
| 72162-1679-0 | 72162167900 | 1000 TABLET in 1 BOTTLE (72162-1679-0) | 1000 tablet | 2023-12-05 | No | No | Historical |
| 72162-1679-1 | 72162167901 | 100 TABLET in 1 BOTTLE (72162-1679-1) | 100 tablet | 2023-12-05 | No | No | Historical |
| 72162-1679-5 | 72162167905 | 500 TABLET in 1 BOTTLE (72162-1679-5) | 500 tablet | 2023-12-05 | No | No | Historical |