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clonidine hydrochloride
clonidine hydrochloride - 29300-135-01 - (clonidine hydrochloride)
Drug Information of clonidine hydrochloride
| Product NDC: | 29300-135 |
| Proprietary Name: | clonidine hydrochloride |
| Non Proprietary Name: | clonidine hydrochloride |
| Active Ingredient(s): | .1 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: | 29300-135 |
| Labeler Name: | Unichem Pharmaceuticals (USA), Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078895 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090921 |
Package Information of clonidine hydrochloride
| Package NDC: | 29300-135-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (29300-135-01) |
NDC Information of clonidine hydrochloride
| NDC Code | 29300-135-01 |
| Proprietary Name | clonidine hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (29300-135-01) |
| Product NDC | 29300-135 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clonidine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090921 |
| Marketing Category Name | ANDA |
| Labeler Name | Unichem Pharmaceuticals (USA), Inc. |
| Substance Name | CLONIDINE HYDROCHLORIDE |
| Strength Number | .1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC] |
