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Anectine
Anectine - 0781-3009-95 - (Succinylcholine Chloride)
Drug Information of Anectine
| Product NDC: | 0781-3009 |
| Proprietary Name: | Anectine |
| Non Proprietary Name: | Succinylcholine Chloride |
| Active Ingredient(s): | 20 mg/mL & nbsp; Succinylcholine Chloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; PARENTERAL |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anectine
| Product NDC: | 0781-3009 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA008453 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19520820 |
Package Information of Anectine
| Package NDC: | 0781-3009-95 |
| Package Description: | 10 VIAL, MULTI-DOSE in 1 CARTON (0781-3009-95) > 10 mL in 1 VIAL, MULTI-DOSE (0781-3009-70) |
NDC Information of Anectine
| NDC Code | 0781-3009-95 |
| Proprietary Name | Anectine |
| Package Description | 10 VIAL, MULTI-DOSE in 1 CARTON (0781-3009-95) > 10 mL in 1 VIAL, MULTI-DOSE (0781-3009-70) |
| Product NDC | 0781-3009 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Succinylcholine Chloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; PARENTERAL |
| Start Marketing Date | 19520820 |
| Marketing Category Name | NDA |
| Labeler Name | Sandoz Inc |
| Substance Name | SUCCINYLCHOLINE CHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Depolarizing Neuromuscular Blocker [EPC],Neuromuscular Depolarizing Blockade [PE] |
