Diltiazem Hydrochloride
- Product NDC
- 63629-7330
- 11-digit product format
- 636297330
- Labeler code
- 63629
- Product ID
- 63629-7330_5408575d-0022-4ee4-a5bd-d87a44020ce2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074185
- Marketing category
- ANDA
- Marketing start
- 1995-12-22
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 90 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-7330-1 | Diltiazem Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 4 |
| 63629-7330-2 | Diltiazem Hydrochloride | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-7330 | DILTIAZEM HYDROCHLORIDE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 4 | Legacy NDC, 2 package rows | 20220115_5408575d-0022-4ee4-a5bd-d87a44020ce2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7330-1 | 63629733001 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7330-1) | 2021-12-22 | 0000-00-00 | No | No | Current |
| 63629-7330-2 | 63629733002 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-7330-2) | 2017-07-18 | 0000-00-00 | No | No | Current |