Details for New Drug Application (NDA): 215488
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NDA 215488 describes METHOHEXITAL SODIUM, which is a drug marketed by Steriscience Speclts and is included in one NDA. It is available from two suppliers. Additional details are available on the METHOHEXITAL SODIUM profile page.
The generic ingredient in METHOHEXITAL SODIUM is methohexital sodium. There are three drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the methohexital sodium profile page.
The generic ingredient in METHOHEXITAL SODIUM is methohexital sodium. There are three drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the methohexital sodium profile page.
Summary for 215488
| Tradename: | METHOHEXITAL SODIUM |
| Applicant: | Steriscience Speclts |
| Ingredient: | methohexital sodium |
| Patents: | 0 |
Suppliers and Packaging for NDA: 215488
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| METHOHEXITAL SODIUM | methohexital sodium | INJECTABLE;INJECTION | 215488 | ANDA | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-893 | 23155-893-31 | 1 VIAL in 1 CARTON (23155-893-31) / 500 mg in 1 VIAL |
| METHOHEXITAL SODIUM | methohexital sodium | INJECTABLE;INJECTION | 215488 | ANDA | ONESOURCE SPECIALTY PHARMA LIMITED | 83270-003 | 83270-003-01 | 500 mg in 1 VIAL (83270-003-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 500MG/VIAL | ||||
| Approval Date: | Oct 3, 2024 | TE: | AP | RLD: | No | ||||
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