Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 008453
Company: SANDOZ
Company: SANDOZ
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| ANECTINE | SUCCINYLCHOLINE CHLORIDE | 500MG/VIAL | INJECTABLE;INJECTION | Discontinued | None | No | No |
| ANECTINE | SUCCINYLCHOLINE CHLORIDE | 20MG/ML | INJECTABLE;INJECTION | Prescription | AP | Yes | Yes |
| ANECTINE | SUCCINYLCHOLINE CHLORIDE | 50MG/ML | INJECTABLE;INJECTION | Discontinued | None | No | No |
| ANECTINE | SUCCINYLCHOLINE CHLORIDE | 1GM/VIAL | INJECTABLE;INJECTION | Discontinued | None | No | No |
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
|---|---|---|---|---|---|
| 11/01/2022 | SUPPL-40 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/008453s040lbl.pdf | |
| 07/26/2018 | SUPPL-36 | Labeling-Package Insert | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/008453s036lbl.pdf | |
| 07/26/2018 | SUPPL-36 | Labeling-Container/Carton Labels | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/008453s036lbl.pdf | |
| 11/22/2010 | SUPPL-27 | Labeling | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/008453s027lbl.pdf |