clonidine hydrochloride
- Product NDC
- 50268-194
- 11-digit product format
- 502680194
- Labeler code
- 50268
- Product ID
- 50268-194_2b48f750-cd85-40fc-e063-6294a90a0299
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA078895
- Marketing category
- ANDA
- Marketing start
- 2023-05-30
- 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 |
|---|
| 50268-194-15 | 50268019415 | 50 BLISTER PACK in 1 BOX (50268-194-15) / 1 TABLET in 1 BLISTER PACK (50268-194-11) | 50 blister pack | 2023-05-30 | No | No | Historical |