Diltiazem Hydrochloride
- Product NDC
- 55154-8140
- 11-digit product format
- 551548140
- Labeler code
- 55154
- Product ID
- 55154-8140_b3424ecb-2370-4b22-9725-92afb0decc0d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA074185
- Marketing category
- ANDA
- Marketing start
- 1995-12-22
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 30 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-8140-0 | 55154814000 | 10 BLISTER PACK in 1 BAG (55154-8140-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 1995-12-22 | 0000-00-00 | No | No | Current |