Succinylcholine Chloride
- Product NDC
- 71872-7251
- 11-digit product format
- 718727251
- Labeler code
- 71872
- Product ID
- 71872-7251_c433d585-6fd4-32ff-e053-2a95a90ab345
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Succinylcholine Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71872-7251 | SUCCINYLCHOLINE CHLORIDE INJECTION, SOLUTION [MEDICAL PURCHASING SOLUTIONS, LLC] | 2 | Legacy NDC | 20230429_c433d585-6fd3-32ff-e053-2a95a90ab345.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71872-7251-1 | 71872725101 | 1 VIAL, MULTI-DOSE in 1 BAG (71872-7251-1) > 10 mL in 1 VIAL, MULTI-DOSE | 2021-05-18 | 0000-00-00 | No | No | Current |