Procainamide Hydrochloride
- Product NDC
- 71872-7353
- 11-digit product format
- 718727353
- Labeler code
- 71872
- Product ID
- 71872-7353_4240554f-94ca-7af2-e063-6294a90a6116
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Procainamide Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC.
- Application
- ANDA218135
- Marketing category
- ANDA
- Marketing start
- 2025-01-15
- Substance
- PROCAINAMIDE HYDROCHLORIDE
- Active strength
- 100 mg/mL
- Pharmacologic classes
- Antiarrhythmic [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 |
|---|
| SI4064O0LX | PROCAINAMIDE HYDROCHLORIDE | 614-39-1 | PROCAINAMIDE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7353-1 | 71872735301 | 1 VIAL in 1 BAG (71872-7353-1) / 10 mL in 1 VIAL | 1 vial | 2025-05-28 | No | No | Historical |