Diltiazem Hydrochloride
- Product NDC
- 60687-562
- 11-digit product format
- 606870562
- Labeler code
- 60687
- Product ID
- 60687-562_c7b7dbce-5d47-055f-e053-2a95a90a9fe8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA211596
- Marketing category
- ANDA
- Marketing start
- 2020-11-04
- Marketing end
- 2022-09-30
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-562-01 | 60687056201 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-562-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-562-11) | 100 blister pack | 2020-10-01 | 0000-00-00 | No | No | Current |