Hydralazine Hydrochloride
- Product NDC
- 71872-7051
- 11-digit product format
- 718727051
- Labeler code
- 71872
- Product ID
- 71872-7051_9ce5ac17-0be9-4c9f-e053-2995a90ae27a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydralazine Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA040730
- Marketing category
- ANDA
- Marketing start
- 2009-05-01
- Marketing end
- 0000-00-00
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE],Arteriolar Vasodilator [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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71872-7051-1 | 71872705101 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7051-1) > 1 mL in 1 VIAL, SINGLE-DOSE | 2018-02-19 | 0000-00-00 | No | No | Current |