Diltiazem Hydrochloride
- Product NDC
- 70518-2241
- 11-digit product format
- 705182241
- Labeler code
- 70518
- Product ID
- 70518-2241_8f033b90-d0a2-6c1e-e053-2995a90aef46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090421
- Marketing category
- ANDA
- Marketing start
- 2019-07-31
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 240 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record