SUCCINYLCHOLINE CHLORIDE
- Product NDC
- 52584-097
- 11-digit product format
- 525840097
- Labeler code
- 52584
- Product ID
- 52584-097_fdc9c193-18be-4427-b163-1da8c2e8ec68
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- succinylcholine chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- ANDA211432
- Marketing category
- ANDA
- Marketing start
- 2019-11-21
- Marketing end
- 2021-06-30
- 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
- 0000-00-00
- 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 |
|---|
| 52584-097-01 | 52584009701 | 1 VIAL, MULTI-DOSE in 1 BAG (52584-097-01) > 10 mL in 1 VIAL, MULTI-DOSE | 2019-11-21 | 2021-06-30 | No | No | Current |