Succinylcholine Chloride
- Product NDC
- 25021-677
- 11-digit product format
- 250210677
- Labeler code
- 25021
- Product ID
- 25021-677_753f28fe-0aa2-42d2-976c-54ac62afb0ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Succinylcholine Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA215022
- Marketing category
- ANDA
- Marketing start
- 2021-10-15
- 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
- 2022-12-31
- 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 |
|---|
| 25021-677-10 | 25021067710 | 25 VIAL in 1 CARTON (25021-677-10) > 10 mL in 1 VIAL | 25 vial | 2021-10-15 | 0000-00-00 | No | No | Current |