clonidine hydrochloride
- Product NDC
- 50090-7009
- 11-digit product format
- 500907009
- Labeler code
- 50090
- Product ID
- 50090-7009_426f0c38-49b6-47b5-b26f-eadb71a801e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078895
- Marketing category
- ANDA
- Marketing start
- 2020-12-24
- 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 |
|---|
| 50090-7009-0 | 50090700900 | 50 BLISTER PACK in 1 BOX (50090-7009-0) / 1 TABLET in 1 BLISTER PACK | 50 blister pack | 2024-01-04 | No | No | Historical |