Succinylcholine Chloride
- Product NDC
- 65219-276
- 11-digit product format
- 652190276
- Labeler code
- 65219
- Product ID
- 65219-276_fdf858c8-71c8-4870-8e5f-baaeb54cde6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Succinylcholine Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Fresenius Kabi USA LLC
- Application
- ANDA217885
- Marketing category
- ANDA
- Marketing start
- 2025-06-19
- Substance
- SUCCINYLCHOLINE CHLORIDE DIHYDRATE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Depolarizing Neuromuscular Blocker [EPC], Neuromuscular Depolarizing Blockade [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Succinylcholine Chloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SUCCINYLCHOLINE CHLORIDE DIHYDRATE | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8L0S1G435E |
| Rxcui | 2694114 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65219-276-01 | Succinylcholine Chloride | 10 mL in 1 SYRINGE, PLASTIC | INJECTION, SOLUTION | 10 | | 5 |
| 65219-276-10 | Succinylcholine Chloride | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | | 5 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 65219-276-01 | 65219027601 | 10 mL in 1 SYRINGE, PLASTIC | 10 ml | | | | Historical |
| 65219-276-10 | 65219027610 | 10 SYRINGE, PLASTIC in 1 CARTON (65219-276-10) / 10 mL in 1 SYRINGE, PLASTIC (65219-276-01) | | 2025-06-19 | No | No | Historical |