SEARCH RESULTS for: Clavulanate potassium (263 results)

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AMOXICILLIN AND CLAVULANATE POTASSIUM tablet, film coated
AMOXICILLIN AND CLAVULANATE POTASSIUM powder, for suspension
AMOXICILLIN AND CLAVULANATE POTASSIUM tablet, chewable

NDC Code(s): 0093-2270-34, 0093-2272-34, 0093-2274-34, 0093-2275-34, view more
0093-2277-73, 0093-2279-73
• Packager: Teva Pharmaceuticals USA, Inc.

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AMOXICILLIN AND CLAVULANATE POTASSIUM tablet, film coated
AMOXICILLIN AND CLAVULANATE POTASSIUM powder, for suspension

NDC Code(s): 69452-334-43, 69452-335-43, 69452-336-11, 69452-337-11
• Packager: Bionpharma Inc.

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AMOXICILLIN AND CLAVULANATE POTASSIUM tablet, film coated
AMOXICILLIN AND CLAVULANATE POTASSIUM powder, for suspension

NDC Code(s): 43598-204-51, 43598-204-52, 43598-204-53, 43598-206-14, view more
43598-206-78, 43598-208-50, 43598-208-51, 43598-208-52, 43598-213-50, 43598-213-51, 43598-213-52, 43598-218-30, 43598-218-78, 43598-221-14, 43598-221-78
• Packager: Dr. Reddy's Laboratories Inc

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AMOXICILLIN AND CLAVULANATE POTASSIUM tablet, film coated
AMOXICILLIN AND CLAVULANATE POTASSIUM powder, for suspension

NDC Code(s): 66685-1001-0, 66685-1001-1, 66685-1002-0, 66685-1002-2, view more
66685-1011-0, 66685-1011-1, 66685-1011-2, 66685-1012-0, 66685-1012-1, 66685-1012-2
• Packager: Sandoz Inc

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AMOXICILLIN AND CLAVULANATE POTASSIUM tablet, film coated

NDC Code(s): 65862-501-05, 65862-501-30, 65862-502-05, 65862-502-20, view more
65862-503-01, 65862-503-20
• Packager: Aurobindo Pharma Limited

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AMOXICILLIN AND CLAVULANATE POTASSIUM tablet, film coated

NDC Code(s): 62135-462-20
• Packager: Chartwell RX, LLC

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AMOXICILLIN AND CLAVULANATE POTASSIUM tablet, film coated

NDC Code(s): 62135-463-20
• Packager: Chartwell RX, LLC

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AMOXICILLIN AND CLAVULANATE POTASSIUM tablet, film coated

NDC Code(s): 16714-295-01, 16714-296-01, 16714-297-01, 16714-297-02
• Packager: NorthStar Rx LLC

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AMOXICILLIN AND CLAVULANATE POTASSIUM tablet, film coated

NDC Code(s): 16714-014-01, 16714-014-02, 16714-476-01, 16714-477-01
• Packager: Northstar RxLLC

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AMOXICILLIN AND CLAVULANATE POTASSIUM tablet

NDC Code(s): 0143-9249-20
• Packager: Hikma Pharmaceuticals USA Inc.

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AMOXICILLIN AND CLAVULANATE POTASSIUM tablet, multilayer, extended release

NDC Code(s): 0781-1943-39, 0781-1943-82
• Packager: Sandoz Inc

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AMOXICILLIN AND POTASSIUM CLAVULANATE powder

NDC Code(s): 73377-026-01, 73377-026-02
• Packager: AX Pharmaceutical Corp

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AMOXICILLAN AND CLAVULANATE POTASSIUM tablet, film coated

NDC Code(s): 51655-158-03
• Packager: Northwind Pharmaceuticals, LLC
• This is a repackaged label.
• Source NDC Code(s): 65862-502

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AMOXICILLIN AND CLAVULANATE POTASSIUM (amoxicillin and clavulanate potassium) tablet, film coated

NDC Code(s): 50090-4604-0, 50090-4604-1, 50090-4604-2, 50090-4604-3, view more
50090-4604-4
• Packager: A-S Medication Solutions
• This is a repackaged label.
• Source NDC Code(s): 42571-161

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AMOXICILLIN AND CLAVULANATE POTASSIUM (amoxicillin and clavulanate potassium) tablet, film coated

NDC Code(s): 53002-2392-1
• Packager: RPK Pharmaceuticals, Inc.
• This is a repackaged label.
• Source NDC Code(s): 42571-161

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AMOXICILLIN AND CLAVULANATE POTASSIUM (amoxicillin and clavulanate potassium) tablet, film coated

NDC Code(s): 53002-7899-1, 53002-7899-2, 53002-7899-4, 53002-7899-6
• Packager: RPK Pharmaceuticals, Inc.
• This is a repackaged label.
• Source NDC Code(s): 42571-162

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AMOXICILLIN AND CLAVULANATE POTASSIUM (amoxicillin and clavulanate potassium) tablet, film coated

NDC Code(s): 53808-0740-1
• Packager: State of Florida DOH Central Pharmacy
• This is a repackaged label.
• Source NDC Code(s): 66685-1001

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AMOXICILLIN AND CLAVULANATE POTASSIUM for suspension

NDC Code(s): 53002-4716-1, 53002-4716-2
• Packager: RPK Pharmaceuticals, Inc.
• This is a repackaged label.
• Source NDC Code(s): 81964-203

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AMOXICILLIN AND CLAVULANATE POTASSIUM powder, for suspension

NDC Code(s): 33261-970-01
• Packager: Aidarex Pharmaceuticals LLC
• This is a repackaged label.
• Source NDC Code(s): 43598-203

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AMOXICILLIN AND CLAVULANATE POTASSIUM powder, for suspension

NDC Code(s): 33261-600-01
• Packager: Aidarex Pharmaceuticals LLC
• This is a repackaged label.
• Source NDC Code(s): 43598-203