SUCCINYLCHOLINE CHLORIDE
- Product NDC
- 52584-377
- 11-digit product format
- 525840377
- Labeler code
- 52584
- Product ID
- 52584-377_1c30d249-c7a8-4ccd-89ed-dd4c25255bb4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- succinylcholine chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- ANDA209467
- Marketing category
- ANDA
- Marketing start
- 2019-01-22
- Marketing end
- 2020-07-31
- 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