Succinylcholine Chloride
- Product NDC
- 49396-0152
- 11-digit product format
- 493960152
- Labeler code
- 49396
- Product ID
- 49396-0152_6e8a325b-92ce-b657-e053-2991aa0a181b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Succinylcholine Chloride
- Dosage form
- INJECTION
- Route
- PARENTERAL
- Labeler
- Renaissance Lakewood LLC
- Application
- ANDA210231
- Marketing category
- ANDA
- Marketing start
- 2018-10-01
- Marketing end
- 0000-00-00
- Substance
- SUCCINYLCHOLINE CHLORIDE
- Active strength
- 200 mg/10mL
- Pharmacologic classes
- Depolarizing Neuromuscular Blocker [EPC],Neuromuscular Depolarizing Blockade [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49396-0152-2 | 49396015202 | 6 CARTON in 1 BOX (49396-0152-2) > 25 VIAL in 1 CARTON > 10 mL in 1 VIAL | 6 carton | 2018-10-01 | 0000-00-00 | No | No | Current |