NDC 69918-700-04 - Succinylcholine Chloride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 69918-700
- Requested NDC
- 69918-700-04
- Package NDCs from labels
- 69918-700-05, 69918-700-12, 69918-700-29, 69918-700-04, 69918-700-11, 69918-700-28, 69918-700-03, 69918-700-27, 69918-700-01, 69918-700-10, 69918-700-25, 69918-700-02, 69918-700-26
- Manufacturer
- Nordic Pharma, Inc. | BIOLOGICAL E. LIMITED
- Effective date
- 2026-01-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Succinylcholine Chloride - Nordic Pharma, Inc. | BIOLOGICAL E. LIMITED | Nordic Pharma, Inc. | BIOLOGICAL E. LIMITED | 2026-01-21 | HUMAN PRESCRIPTION DRUG LABEL |
| Succinylcholine Chloride - Medical Purchasing Solutions, LLC | Medical Purchasing Solutions, LLC | 2023-05-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Succinylcholine Chloride - Amring Pharmaceuticals Inc. | INDOCO REMEDIES LIMITED | Amring Pharmaceuticals Inc. | INDOCO REMEDIES LIMITED | 2023-04-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Succinylcholine Chloride - Amring Pharmaceuticals Inc. | INDOCO REMEDIES LIMITED | Amring Pharmaceuticals Inc. | INDOCO REMEDIES LIMITED | 2022-12-13 | HUMAN PRESCRIPTION DRUG LABEL |
| SUCCINYLCHOLINE - Amring Pharmaceuticals Inc. | Renaissance Lakewood LLC | Amring Pharmaceuticals Inc. | Renaissance Lakewood LLC | 2022-06-03 | HUMAN PRESCRIPTION DRUG LABEL |
| SUCCINYLCHOLINE - Amring Pharmaceuticals Inc. | Renaissance Lakewood LLC | Amring Pharmaceuticals Inc. | Renaissance Lakewood LLC | 2022-06-03 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69918-700-01 | Succinylcholine Chloride | 10 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 10 | 6 | |
| 69918-700-10 | Succinylcholine Chloride | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | 6 | |
| 69918-700-25 | Succinylcholine Chloride | 25 in 1 CARTON | INJECTION, SOLUTION | 25 | 6 | |
| 69918-700-05 | Succinylcholine Chloride | 10 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 10 | 1 | |
| 69918-700-12 | Succinylcholine Chloride | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | 1 | |
| 69918-700-29 | Succinylcholine Chloride | 25 in 1 CARTON | INJECTION, SOLUTION | 25 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Ringers | SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE, | Baxter Healthcare Corporation | e1953d54-818d-46a6-8532-518ebae6d84e | 2012-06-13 | 451W47IQ8X | |
| Lactated Ringers | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE | Baxter Healthcare Corporation | f09f80bf-2f8b-4420-865d-aec2d5e5cd4d | 2012-06-12 | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.