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Pioglitazone Hydrochloride
Pioglitazone Hydrochloride - 68084-630-01 - (pioglitazone hydrochloride)
Drug Information of Pioglitazone Hydrochloride
| Product NDC: | 68084-630 |
| Proprietary Name: | Pioglitazone Hydrochloride |
| Non Proprietary Name: | pioglitazone hydrochloride |
| Active Ingredient(s): | 30 mg/1 & nbsp; pioglitazone hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pioglitazone Hydrochloride
| Product NDC: | 68084-630 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021073 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130625 |
Package Information of Pioglitazone Hydrochloride
| Package NDC: | 68084-630-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-630-01) > 10 TABLET in 1 BLISTER PACK (68084-630-11) |
NDC Information of Pioglitazone Hydrochloride
| NDC Code | 68084-630-01 |
| Proprietary Name | Pioglitazone Hydrochloride |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-630-01) > 10 TABLET in 1 BLISTER PACK (68084-630-11) |
| Product NDC | 68084-630 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | pioglitazone hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130625 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | American Health Packaging |
| Substance Name | PIOGLITAZONE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC],Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [Chemical/Ingredient],PPAR gamma [Chemical/Ingredient],Thiazolidinedione [EPC],Thiazolidinediones [Chemical/Ingredient] |
