Succinylcholine Chloride
- Product NDC
- 0641-6234
- 11-digit product format
- 006416234
- Labeler code
- 0641
- Product ID
- 0641-6234_87fa35fa-32d3-4542-9e08-8ecb0999754d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Succinylcholine Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- NDA215143
- Marketing category
- NDA
- Marketing start
- 2022-03-17
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0641-6234 | SUCCINYLCHOLINE CHLORIDE INJECTION, SOLUTION [HIKMA PHARMACEUTICALS USA INC.] | 6 | Legacy NDC | 20240412_cb5b3361-9099-4a12-b545-f1e50b0781dd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0641-6234-10 | 00641623410 | 10 SYRINGE, PLASTIC in 1 CARTON (0641-6234-10) > 5 mL in 1 SYRINGE, PLASTIC | 2022-03-17 | 0000-00-00 | No | No | Current |