PROCAINAMIDE HYDROCHLORIDE
- Product NDC
- 0404-9939
- 11-digit product format
- 004049939
- Labeler code
- 0404
- Product ID
- 0404-9939_383e9af9-8cef-4e1e-a3a6-a1b947dcb024
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- procainamide hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Henry Schein, Inc.
- Application
- ANDA089069
- Marketing category
- ANDA
- Marketing start
- 2022-01-13
- Marketing end
- 0000-00-00
- Substance
- PROCAINAMIDE HYDROCHLORIDE
- Active strength
- 500 mg/mL
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0404-9939-02 | 00404993902 | 1 VIAL, MULTI-DOSE in 1 BAG (0404-9939-02) > 2 mL in 1 VIAL, MULTI-DOSE | 2022-01-13 | 0000-00-00 | No | No | Current |