SUCCINYLCHOLINE CHLORIDE
- Product NDC
- 71872-7263
- 11-digit product format
- 718727263
- Labeler code
- 71872
- Product ID
- 71872-7263_d162934c-67c8-6e78-e053-2a95a90ac443
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SUCCINYLCHOLINE CHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA211432
- Marketing category
- ANDA
- Marketing start
- 2020-08-31
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71872-7263-1 | 71872726301 | 1 VIAL, MULTI-DOSE in 1 BAG (71872-7263-1) > 10 mL in 1 VIAL, MULTI-DOSE | 2021-08-17 | 0000-00-00 | No | No | Current |