Succinylcholine Chloride
- Product NDC
- 0548-9801
- 11-digit product format
- 005489801
- Labeler code
- 0548
- Product ID
- 0548-9801_7dee0a04-5d90-4d23-b87d-f20dfb8fd5f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Succinylcholine Chloride
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Amphastar Pharmaceuticals, Inc.
- Application
- ANDA213432
- Marketing category
- ANDA
- Marketing start
- 2020-12-01
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record