United States · FDA National Drug Code directory
isosorbide dinitrate and hydralazine hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 73141-012_339fc165-a47c-e0e1-e063-6394a90a4622
- Product NDC
- 73141-012
- Form
- TABLET, FILM COATED
- Composition / generic term
- isosorbide dinitrate and hydralazine hydrochloride
- Labeler
- A2A Integrated Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240422
- Source listing expiry
- 20261231
Source-listed ingredients
- ISOSORBIDE DINITRATE — 20 mg/1
- HYDRALAZINE HYDROCHLORIDE — 37.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET, FILM COATED in 1 BOTTLE (73141-012-03) · 73141-012-03
- 180 TABLET, FILM COATED in 1 BOTTLE (73141-012-18) · 73141-012-18
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →