Hydralazine Hydrochloride
- Product NDC
- 55154-9367
- 11-digit product format
- 551549367
- Labeler code
- 55154
- Product ID
- 55154-9367_61fae8d4-7897-4cc1-8385-39ea58bd1c8d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HYDRALAZINE HYDROCHLORIDE
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Cardinal Health
- Application
- ANDA040388
- Marketing category
- ANDA
- Marketing start
- 2011-01-31
- Marketing end
- 2021-08-31
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-9367-5 | 55154936705 | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-9367-5) > 1 mL in 1 VIAL, SINGLE-DOSE | 2011-01-31 | 2021-08-31 | No | No | Current |