Succinylcholine Chloride
- Product NDC
- 14789-104
- 11-digit product format
- 147890104
- Labeler code
- 14789
- Product ID
- 14789-104_3fe64c8a-f229-486d-8f7a-86b8893b7b9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Succinylcholine Chloride
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Nexus Pharmaceuticals Inc
- Application
- ANDA213552
- Marketing category
- ANDA
- Marketing start
- 2021-01-11
- Marketing end
- 0000-00-00
- Substance
- SUCCINYLCHOLINE CHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Depolarizing Neuromuscular Blocker [EPC], Neuromuscular Depolarizing Blockade [PE]
- 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 |
|---|
| 14789-104-05 | 14789010405 | 25 VIAL, MULTI-DOSE in 1 TRAY (14789-104-05) > 10 mL in 1 VIAL, MULTI-DOSE (14789-104-07) | 2021-01-11 | 0000-00-00 | No | No | Current |