SUCCINYLCHOLINE CHLORIDE
- Product NDC
- 68001-448
- 11-digit product format
- 680010448
- Labeler code
- 68001
- Product ID
- 68001-448_e7235c4d-af7b-2cc5-e053-2a95a90aa318
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SUCCINYLCHOLINE CHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- BluePoint Laboratories
- 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
- 2023-12-31
- 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 |
|---|
| 68001-448-60 | 68001044860 | 25 VIAL, MULTI-DOSE in 1 CARTON (68001-448-60) > 10 mL in 1 VIAL, MULTI-DOSE (68001-448-28) | 2020-08-31 | 0000-00-00 | No | No | Current |