| NDC Code: |
52125-504 |
| Proprietary Name: |
Diltiazem HydrochlorideExtended Release |
| Suffix: |
Extended Release |
| Non-Proprietary Name: |
Diltiazem Hydrochloride |
| Dosage Form: |
CAPSULE, COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
22-05-2013 |
| Category Name: |
ANDA |
| Application Number: |
ANDA074984 |
| Labeler: |
REMEDYREPACK INC. |
| Substance Name: |
DILTIAZEM HYDROCHLORIDE |
| Active Numerator Strength: |
240 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
| DEA Schedule: |
|
