Diltiazem Hydrochloride
- Product NDC
- 58118-1007
- 11-digit product format
- 581181007
- Labeler code
- 58118
- Product ID
- 58118-1007_b0254329-5d8a-b309-e053-2995a90a8411
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- Application
- NDA018602
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2010-12-25
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58118-1007 | DILTIAZEM HYDROCHLORIDE TABLET [CLINICAL SOLUTIONS WHOLESALE, LLC] | 4 | Legacy NDC | 20200926_ad4cb6e0-8dc5-4fbc-9ea1-6ec64e4b2f4f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58118-1007-8 | 58118100708 | 30 TABLET in 1 BLISTER PACK (58118-1007-8) | 30 tablet | 2018-02-07 | 0000-00-00 | No | No | Current |