Hydralazine Hydrochloride
- Product NDC
- 65084-127
- 11-digit product format
- 650840127
- Labeler code
- 65084
- Product ID
- 65084-127_bb027e1d-05ae-bfd2-e053-2995a90a7a10
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydralazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba RX Pak
- Application
- ANDA088468
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Marketing end
- 2021-11-30
- Substance
- HYDRALAZINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65084-127-10 | 65084012710 | 10 BLISTER PACK in 1 BOX (65084-127-10) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2019-06-19 | 2021-11-30 | No | No | Current |