NDC 47335-676 – Diltiazem Hydrochloride
Diltiazem Hydrochloride 180 mg/1 · Capsule, Extended Release · Oral
Product NDC47335-676
Product details
- Brand name
- Diltiazem Hydrochloride
- Generic name
- Diltiazem Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090492
- Marketed since
- October 31, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Calcium Channel Blocker
Active ingredients
- Diltiazem Hydrochloride 180 mg/1
Uses, dosage, side effects and warnings for Diltiazem Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 47335-676-13 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-676-13) | Oct 31, 2011 |
| 47335-676-18 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-676-18) | Oct 31, 2011 |
| 47335-676-19 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-676-19) | Oct 31, 2011 |
| 47335-676-81 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-676-81) | Oct 31, 2011 |
| 47335-676-83 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-676-83) | Oct 31, 2011 |
Recalls mentioning this NDC
- D-0262-2023 Feb 8, 2023 · Class II
Failed Impurity (Deacetyl Diltiazem Hydrochloride) specification during stability testing and failed dissolution testing at FDA laboratory.
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