Diltiazem Hydrochloride
- Product NDC
- 50436-6126
- 11-digit product format
- 504366126
- Labeler code
- 50436
- Product ID
- 50436-6126_2c551417-a2d1-487c-8a24-dbbba526ff65
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA074984
- Marketing category
- ANDA
- Marketing start
- 1999-12-20
- 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
- 2019-12-31
- 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 |
|---|
| 50436-6126-1 | Diltiazem Hydrochloride | 30 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-6126 | DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [UNIT DOSE SERVICES] | 2 | Legacy NDC, 1 package rows | 20130520_6e01e824-07b5-4a88-a31f-b5d673c51701.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-6126-1 | 50436612601 | 30 in 1 BOTTLE | Historical |