Bretylium Tosylate
- Product NDC
- 62559-870
- 11-digit product format
- 625590870
- Labeler code
- 62559
- Product ID
- 62559-870_04048ad4-2e59-4456-9db0-1beac8f775aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bretylium tosylate
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA204386
- Marketing category
- ANDA
- Marketing start
- 2019-12-11
- Marketing end
- 0000-00-00
- Substance
- BRETYLIUM TOSYLATE
- Active strength
- 50 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62559-870-11 | 62559087011 | 10 mL in 1 VIAL, SINGLE-DOSE (62559-870-11) | 10 ml | 2019-12-11 | 0000-00-00 | No | No | Current |