NDC 0093-0318 – Diltiazem Hydrochloride
Diltiazem Hydrochloride 30 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-0318
Product details
- Brand name
- Diltiazem Hydrochloride
- Generic name
- Diltiazem Hydrochloride
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA074185
- Marketed since
- December 22, 1995
- Listing expires
- December 31, 2026
- Pharmacologic class
- Calcium Channel Blocker
Active ingredients
- Diltiazem Hydrochloride 30 mg/1
Uses, dosage, side effects and warnings for Diltiazem Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0093-0318-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-0318-01) | Dec 22, 1995 |
| 0093-0318-05 | 500 TABLET, FILM COATED in 1 BOTTLE (0093-0318-05) | Dec 28, 1995 |
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