Details for New Drug Application (NDA): 090583
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The generic ingredient in AMPICILLIN SODIUM is ampicillin sodium. There are seventy drug master file entries for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the ampicillin sodium profile page.
Summary for 090583
Tradename: | AMPICILLIN SODIUM |
Applicant: | Sagent Pharms Inc |
Ingredient: | ampicillin sodium |
Patents: | 0 |
Suppliers and Packaging for NDA: 090583
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
AMPICILLIN SODIUM | ampicillin sodium | INJECTABLE;INJECTION | 090583 | ANDA | Medical Purchasing Solutions, LLC | 71872-7280 | 71872-7280-1 | 1 VIAL in 1 BAG (71872-7280-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
AMPICILLIN SODIUM | ampicillin sodium | INJECTABLE;INJECTION | 090583 | ANDA | Medical Purchasing Solutions, LLC | 71872-7286 | 71872-7286-1 | 1 VIAL in 1 BAG (71872-7286-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 125MG BASE/VIAL | ||||
Approval Date: | Nov 27, 2015 | TE: | AP | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 250MG BASE/VIAL | ||||
Approval Date: | Nov 27, 2015 | TE: | AP | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 500MG BASE/VIAL | ||||
Approval Date: | Nov 27, 2015 | TE: | AP | RLD: | No |
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