| NDC Code |
35356-723-20 |
| Proprietary Name |
CLONIDINE HYDROCHLORIDE |
| Package Description |
20 TABLET in 1 BOTTLE (35356-723-20) |
| Product NDC |
35356-723 |
| Product Type Name |
HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name |
clonidine hydrochloride |
| Dosage Form Name |
TABLET |
| Route Name |
ORAL |
| Start Marketing Date |
19870904 |
| Marketing Category Name |
ANDA |
| Labeler Name |
Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
| Substance Name |
CLONIDINE HYDROCHLORIDE |
| Strength Number |
.1 |
| Strength Unit |
mg/1 |
| Pharmaceutical Classes |
Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |