Product NDC: | 0093-0318 |
Proprietary Name: | Diltiazem Hydrochloride |
Non Proprietary Name: | Diltiazem Hydrochloride |
Active Ingredient(s): | 30 mg/1 & nbsp; Diltiazem Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0093-0318 |
Labeler Name: | Teva Pharmaceuticals USA Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074185 |
Marketing Category: | ANDA |
Start Marketing Date: | 19951222 |
Package NDC: | 0093-0318-05 |
Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE (0093-0318-05) |
NDC Code | 0093-0318-05 |
Proprietary Name | Diltiazem Hydrochloride |
Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (0093-0318-05) |
Product NDC | 0093-0318 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Diltiazem Hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19951222 |
Marketing Category Name | ANDA |
Labeler Name | Teva Pharmaceuticals USA Inc |
Substance Name | DILTIAZEM HYDROCHLORIDE |
Strength Number | 30 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |