SUCCINYLCHOLINE CHLORIDE
- Product NDC
- 51991-964
- 11-digit product format
- 519910964
- Labeler code
- 51991
- Product ID
- 51991-964_1ab08787-3795-4f00-ba67-484efecc0608
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- succinylcholine chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Application
- ANDA212638
- Marketing category
- ANDA
- Marketing start
- 2020-03-01
- Marketing end
- 2023-03-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51991-964-25 | 51991096425 | 25 VIAL, MULTI-DOSE in 1 CARTON (51991-964-25) > 10 mL in 1 VIAL, MULTI-DOSE (51991-964-99) | 2020-03-01 | 0000-00-00 | No | No | Current |