Succinylcholine Chloride
- Product NDC
- 52584-964
- 11-digit product format
- 525840964
- Labeler code
- 52584
- Product ID
- 52584-964_305835da-7a6f-4909-b915-2ba40fd6bb0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Succinylcholine Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA212638
- Marketing category
- ANDA
- Marketing start
- 2020-10-21
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-964-99 | 52584096499 | 1 VIAL, MULTI-DOSE in 1 BAG (52584-964-99) > 10 mL in 1 VIAL, MULTI-DOSE | 2020-10-21 | 0000-00-00 | No | No | Current |