Clonidine Hydrochloride
- Product NDC
- 72162-1681
- 11-digit product format
- 721621681
- Labeler code
- 72162
- Product ID
- 72162-1681_a81f5bc2-a959-40fd-ab09-46dbe5258bad
- 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 |
|---|
| 72162-1681-0 | 72162168100 | 1000 TABLET in 1 BOTTLE (72162-1681-0) | 1000 tablet | 2023-10-03 | No | No | Historical |
| 72162-1681-1 | 72162168101 | 100 TABLET in 1 BOTTLE (72162-1681-1) | 100 tablet | 2023-10-03 | No | No | Historical |
| 72162-1681-5 | 72162168105 | 500 TABLET in 1 BOTTLE (72162-1681-5) | 500 tablet | 2023-10-03 | No | No | Historical |