Succinylcholine Chloride
- Product NDC
- 16729-493
- 11-digit product format
- 167290493
- Labeler code
- 16729
- Product ID
- 16729-493_cf7d823f-75ae-91a7-e053-2995a90a4932
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Succinylcholine Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Accord Healthcare, Inc.
- Application
- ANDA213705
- Marketing category
- ANDA
- Marketing start
- 2021-04-07
- 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 |
|---|
| 16729-493-45 | 16729049345 | 10 VIAL, MULTI-DOSE in 1 CARTON (16729-493-45) > 10 mL in 1 VIAL, MULTI-DOSE | 2021-04-07 | 0000-00-00 | No | No | Current |