Home
>
National Drug Code (NDC)
>
Diltiazem Hydrochloride
Diltiazem Hydrochloride - 47335-669-19 - (Diltiazem Hydrochloride)
Drug Information of Diltiazem Hydrochloride
| Product NDC: | 47335-669 |
| Proprietary Name: | Diltiazem Hydrochloride |
| Non Proprietary Name: | Diltiazem Hydrochloride |
| Active Ingredient(s): | 120 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: | 47335-669 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090421 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101115 |
Package Information of Diltiazem Hydrochloride
| Package NDC: | 47335-669-19 |
| Package Description: | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-669-19) |
NDC Information of Diltiazem Hydrochloride
| NDC Code | 47335-669-19 |
| Proprietary Name | Diltiazem Hydrochloride |
| Package Description | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-669-19) |
| Product NDC | 47335-669 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diltiazem Hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20101115 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | DILTIAZEM HYDROCHLORIDE |
| Strength Number | 120 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
