SEARCH RESULTS for: thiotepa (94 results)

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THIOTEPA INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

NDC Code(s): 68083-446-01, 68083-503-01
• Packager: GLAND PHARMA LIMITED

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THIOTEPA INJECTION, POWDER, FOR SOLUTION

NDC Code(s): 71288-156-05, 71288-157-10
• Packager: MEITHEAL PHARMACEUTICALS INC

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THIOTEPA INJECTION, POWDER, FOR SOLUTION

NDC Code(s): 69539-123-01, 69539-124-01
• Packager: MSN LABORATORIES PRIVATE LIMITED

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THIOTEPA INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

NDC Code(s): 72205-045-01, 72205-046-01
• Packager: NOVADOZ PHARMACEUTICALS LLC

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TEPADINA (THIOTEPA) INJECTION, POWDER, FOR SOLUTION

NDC Code(s): 70121-1630-1, 70121-1631-1
• Packager: AMNEAL PHARMACEUTICALS LLC

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THIOTEPA INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

NDC Code(s): 0143-9292-01
• Packager: HIKMA PHARMACEUTICALS USA INC.

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THIOTEPA INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

NDC Code(s): 65219-029-20
• Packager: FRESENIUS KABI USA, LLC

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THIOTEPA INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

NDC Code(s): 43598-171-11
• Packager: DR.REDDY'S LABORATORIES INC.,

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THIOTEPA INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

NDC Code(s): 0143-9565-01
• Packager: HIKMA PHARMACEUTICALS USA INC.

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THIOTEPA INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

NDC Code(s): 54879-014-13
• Packager: STI PHARMA LLC

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THIOTEPA INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

NDC Code(s): 25021-246-02
• Packager: SAGENT PHARMACEUTICALS

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THIOTEPA INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

NDC Code(s): 0143-9309-01
• Packager: HIKMA PHARMACEUTICALS USA INC.

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THIOTEPA INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

NDC Code(s): 43598-650-11
• Packager: DR.REDDY'S LABORATORIES INC.,

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THIOTEPA INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

NDC Code(s): 70860-220-02
• Packager: ATHENEX PHARMACEUTICAL DIVISION, LLC.

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BUPROPION HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 43353-538-16, 43353-538-82, 43353-546-30, 43353-546-60, view more
43353-546-80
• Packager: APHENA PHARMA SOLUTIONS - TENNESSEE, LLC
• This is a repackaged label.
• Source NDC Code(s): 0591-3540, 0591-3541

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BUPROPION HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 53808-0213-1
• Packager: STATE OF FLORIDA DOH CENTRAL PHARMACY
• This is a repackaged label.
• Source NDC Code(s): 0093-0280

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BUPROPION HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 67046-075-30, 67046-076-30
• Packager: CONTRACT PHARMACY SERVICES-PA
• This is a repackaged label.
• Source NDC Code(s): 0378-0433, 0378-0435

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BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE

NDC Code(s): 21695-019-60, 21695-020-60, 21695-295-30, 21695-295-60
• Packager: REBEL DISTRIBUTORS CORP.
• This is a repackaged label.
• Source NDC Code(s): 0591-3540, 0591-3541, 0591-3542

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BUDEPRION (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 16590-589-30, 16590-589-60, 16590-589-90
• Packager: STAT RX USA LLC
• This is a repackaged label.
• Source NDC Code(s): 10370-101

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BUPROPION HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 53808-0214-1
• Packager: STATE OF FLORIDA DOH CENTRAL PHARMACY
• This is a repackaged label.
• Source NDC Code(s): 0378-0435