Home
>
National Drug Code (NDC)
>
Diltiazem Hydrochloride
Diltiazem Hydrochloride - 51079-948-08 - (diltiazem hydrochloride)
Drug Information of Diltiazem Hydrochloride
| Product NDC: | 51079-948 |
| Proprietary Name: | Diltiazem Hydrochloride |
| Non Proprietary Name: | diltiazem hydrochloride |
| Active Ingredient(s): | 180 mg/1 & nbsp; diltiazem hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diltiazem Hydrochloride
| Product NDC: | 51079-948 |
| Labeler Name: | Mylan Institutional Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075124 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120427 |
Package Information of Diltiazem Hydrochloride
| Package NDC: | 51079-948-08 |
| Package Description: | 80 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-948-08) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (51079-948-01) |
NDC Information of Diltiazem Hydrochloride
| NDC Code | 51079-948-08 |
| Proprietary Name | Diltiazem Hydrochloride |
| Package Description | 80 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-948-08) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (51079-948-01) |
| Product NDC | 51079-948 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | diltiazem hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120427 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Institutional Inc. |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
