HydrALAZINE hydrochloride
- Product NDC
- 71872-7274
- 11-digit product format
- 718727274
- Labeler code
- 71872
- Product ID
- 71872-7274_facb9282-cc50-7e82-e053-6294a90af0aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- HydrALAZINE hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA213667
- Marketing category
- ANDA
- Marketing start
- 2020-12-18
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| FD171B778Y | HYDRALAZINE HYDROCHLORIDE | 304-20-1 | HYDRALAZINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7274-1 | 71872727401 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7274-1) / 20 mL in 1 VIAL, SINGLE-DOSE | 2021-12-09 | No | No | Historical |