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CLONIDINE HYDROCHLORIDE
CLONIDINE HYDROCHLORIDE - 53489-217-01 - (clonidine hydrochloride)
Drug Information of CLONIDINE HYDROCHLORIDE
| Product NDC: | 53489-217 |
| Proprietary Name: | CLONIDINE HYDROCHLORIDE |
| Non Proprietary Name: | clonidine hydrochloride |
| Active Ingredient(s): | .3 mg/1 & nbsp; clonidine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CLONIDINE HYDROCHLORIDE
| Product NDC: | 53489-217 |
| Labeler Name: | Mutual Pharmaceutical Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070923 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19870904 |
Package Information of CLONIDINE HYDROCHLORIDE
| Package NDC: | 53489-217-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (53489-217-01) |
NDC Information of CLONIDINE HYDROCHLORIDE
| NDC Code | 53489-217-01 |
| Proprietary Name | CLONIDINE HYDROCHLORIDE |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (53489-217-01) |
| Product NDC | 53489-217 |
| 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 | Mutual Pharmaceutical Company, Inc. |
| Substance Name | CLONIDINE HYDROCHLORIDE |
| Strength Number | .3 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |
