PROCAINAMIDE HYDROCHLORIDE
- Product NDC
- 52584-106
- 11-digit product format
- 525840106
- Labeler code
- 52584
- Product ID
- 52584-106_6918f728-6c39-4be9-b0f6-6eb5f12bbcaf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- procainamide hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables and Vaccines, INC
- Application
- ANDA089069
- Marketing category
- ANDA
- Marketing start
- 2021-02-18
- Marketing end
- 0000-00-00
- Substance
- PROCAINAMIDE HYDROCHLORIDE
- Active strength
- 500 mg/mL
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 52584-106-41 | 52584010641 | 1 VIAL, MULTI-DOSE in 1 BAG (52584-106-41) > 2 mL in 1 VIAL, MULTI-DOSE | 2021-02-18 | 0000-00-00 | No | No | Current |