SEARCH RESULTS for: Antirheumatic Agent [Drug Class] (100 results)

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 83980-001-01, 83980-001-05, 83980-001-10, 83980-001-97
• Packager: Ipca Laboratories Limited

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 42385-971-01, 42385-971-05, 42385-971-11, 42385-971-60
• Packager: Laurus Labs Limited

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HYDROXYCHLOROQUINESULFATE tablet, film coated

NDC Code(s): 68180-120-01, 68180-120-02
• Packager: Lupin Pharmaceuticals, Inc.

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 0904-7046-06, 0904-7046-61
• Packager: Major Pharmaceuticals
• This is a repackaged label.
• Source NDC Code(s): 43598-721

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 0615-8459-39
• Packager: NCS HealthCare of KY, LLC dba Vangard Labs
• This is a repackaged label.
• Source NDC Code(s): 68382-096

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 16714-110-01, 16714-110-02
• Packager: Northstar Rx LLC.

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 68071-2912-2, 68071-2912-3, 68071-2912-9
• Packager: NuCare Pharmaceuticals,Inc.
• This is a repackaged label.
• Source NDC Code(s): 68382-096

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 68071-2332-1
• Packager: NuCare Pharmaceuticals,Inc.
• This is a repackaged label.
• Source NDC Code(s): 16714-110

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 68788-7747-2, 68788-7747-3
• Packager: Preferred Pharmaceuticals, Inc.
• This is a repackaged label.
• Source NDC Code(s): 68382-096

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 82009-045-05
• Packager: Quallent Pharmaceuticals Health LLC

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 67296-1780-1
• Packager: RedPharm Drug, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0781-5994

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 16571-112-01, 16571-112-06, 16571-112-10, 16571-112-50
• Packager: Rising Pharma Holdings, Inc.

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 53002-4850-2, 53002-4850-6
• Packager: RPK Pharmaceuticals, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0591-3041

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 0093-2401-01
• Packager: Teva Pharmaceuticals USA, Inc.

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 65841-633-01, 65841-633-05, 65841-633-30
• Packager: Zydus Lifesciences Limited

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HYDROXYCHLOROQUINE SULFATE tablet, film coated

NDC Code(s): 68382-096-01, 68382-096-05, 68382-096-30, 68382-096-77
• Packager: Zydus Pharmaceuticals USA Inc.

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HYDROXYCHLOROQUINE SULFATE tablet

NDC Code(s): 57664-761-13, 57664-761-88
• Packager: Sun Pharmaceutical Industries, Inc.

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HYDROXYCHLOROQUINE tablet

NDC Code(s): 62135-752-90
• Packager: Chartwell RX, LLC

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LEFLUNICLO (leflunomide and diclofenac sodium gel) kit

NDC Code(s): 0113-1189-01, 70748-130-06, 72835-602-02
• Packager: V2 Pharma, LLC

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LEFLUNOMIDE powder

NDC Code(s): 73309-075-01, 73309-075-02, 73309-075-03, 73309-075-04
• Packager: BLUEBAY SHANDONG CO.,LTD