SEARCH RESULTS for: CHI530446X (285 results)

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DEPAKOTE (DIVALPROEX SODIUM) TABLET, DELAYED RELEASE

NDC Code(s): 0074-6212-13, 0074-6214-13, 0074-6214-53, 0074-6215-13, view more
0074-6215-53, 0074-7325-13, 0074-7326-13, 0074-7327-13
• Packager: ABBVIE INC.

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VALSARTAN AND HYDROCHLOROTHIAZIDE TABLET, FILM COATED

NDC Code(s): 0378-6321-05, 0378-6321-77, 0378-6322-05, 0378-6322-77, view more
0378-6323-05, 0378-6323-77, 0378-6324-05, 0378-6324-77, 0378-6325-05, 0378-6325-77
• Packager: MYLAN PHARMACEUTICALS INC.

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K-TAB (POTASSIUM CHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 0074-3023-13, 0074-3023-53, 0074-3058-41, 0074-3058-46, view more
0074-3278-13, 0074-3278-19, 0074-7804-13, 0074-7804-19
• Packager: ABBVIE INC.

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CIMETIDINE TABLET, FILM COATED

NDC Code(s): 0378-0053-01, 0378-0317-01, 0378-0372-01, 0378-0541-01
• Packager: MYLAN PHARMACEUTICALS INC.

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VALSARTAN TABLET, FILM COATED

NDC Code(s): 0378-5807-93, 0378-5813-77, 0378-5814-77, 0378-5815-77
• Packager: MYLAN PHARMACEUTICALS INC.

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MENEST (ESTERIFIED ESTROGENS) TABLET, FILM COATED

NDC Code(s): 61570-072-01, 61570-073-01, 61570-074-01, 61570-075-50
• Packager: PFIZER LABORATORIES DIV PFIZER INC

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POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s): 68382-320-01, 68382-320-10, 68382-398-01, 68382-398-05, view more
68382-600-01, 68382-600-10, 68382-776-01, 68382-776-10
• Packager: ZYDUS PHARMACEUTICALS USA INC

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ALPRAZOLAM TABLET, ORALLY DISINTEGRATING

NDC Code(s): 49884-110-74, 49884-111-74, 49884-213-74, 49884-214-74
• Packager: PAR PHARMACEUTICAL, INC.

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MENEST (ESTROGENS, ESTERIFIED) TABLET

NDC Code(s): 54868-5934-0, 54868-5934-1, 54868-6211-0, 54868-6211-1, view more
54868-6212-0, 54868-6212-1
• Packager: PHYSICIANS TOTAL CARE, INC.
• This is a repackaged label.
• Source NDC Code(s): 61570-072-01, 61570-073-01, 61570-074-01

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BIAXIN (CLARITHROMYCIN) TABLET, FILM COATED BIAXIN (CLARITHROMYCIN) TABLET, FILM COATED, EXTENDED RELEASE BIAXIN (CLARITHROMYCIN) GRANULE, FOR SUSPENSION

NDC Code(s): 54868-2338-0, 54868-2338-1, 54868-2338-2, 54868-2338-3, view more
54868-2338-4, 54868-2338-5, 54868-2338-6, 54868-2338-7, 54868-3384-0, 54868-3820-0, 54868-3820-1, 54868-4191-0, 54868-4191-1, 54868-4919-0
• Packager: PHYSICIANS TOTAL CARE, INC.
• This is a repackaged label.
• Source NDC Code(s): 0074-2586, 0074-3163, 0074-3165, 0074-3188, view more
  0074-3368

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SERTRALINE TABLET, FILM COATED

NDC Code(s): 0904-6924-61, 0904-6925-61, 0904-6926-61
• Packager: MAJOR PHARMACEUTICALS
• This is a repackaged label.
• Source NDC Code(s): 68180-351, 68180-352, 68180-353

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DIVALPROEX SODIUM TABLET, DELAYED RELEASE

NDC Code(s): 0615-8326-39, 0615-8327-30, 0615-8327-39, 0615-8328-30, view more
0615-8328-39
• Packager: NCS HEALTHCARE OF KY, LLC DBA VANGARD LABS
• This is a repackaged label.
• Source NDC Code(s): 0832-7122, 0832-7123, 0832-7124

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DIVALPROEX SODIUM TABLET, DELAYED RELEASE

NDC Code(s): 65862-402-01, 65862-402-05, 65862-402-10, 65862-402-39, view more
65862-402-99, 65862-403-01, 65862-403-05, 65862-403-10, 65862-403-22, 65862-959-01, 65862-959-05, 65862-959-10, 65862-959-71, 65862-959-99
• Packager: AUROBINDO PHARMA LIMITED

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SERTRALINE TABLET, FILM COATED

NDC Code(s): 68180-351-01, 68180-351-03, 68180-351-06, 68180-351-08, view more
68180-351-09, 68180-352-01, 68180-352-02, 68180-352-03, 68180-352-05, 68180-352-06, 68180-352-09, 68180-352-11, 68180-353-01, 68180-353-02, 68180-353-03, 68180-353-05, 68180-353-06, 68180-353-09, 68180-353-11
• Packager: LUPIN PHARMACEUTICALS, INC.

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SERTRALINE TABLET, FILM COATED

NDC Code(s): 50268-768-11, 50268-768-15, 50268-769-11, 50268-769-15, view more
50268-770-11, 50268-770-15
• Packager: AVPAK
• This is a repackaged label.
• Source NDC Code(s): 68180-351, 68180-352, 68180-353

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DIVALPROEX SODIUM TABLET, DELAYED RELEASE

NDC Code(s): 29300-138-01, 29300-138-05, 29300-138-10, 29300-139-01, view more
29300-139-05, 29300-139-10, 29300-140-01, 29300-140-05, 29300-140-10
• Packager: UNICHEM PHARMACEUTICALS (USA), INC.

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OLIKA HAND SANITIZER ORANGE BLOSSOM (ETHYL ALCOHOL) LIQUID OLIKA HAND SANITIZER LAVENDER (ETHYL ALCOHOL) LIQUID OLIKA HAND SANITIZER CHARCOAL (ETHYL ALCOHOL) LIQUID OLIKA HAND SANITIZER CUCUMBER BASIL (ETHYL ALCOHOL) LIQUID OLIKA HAND SANITIZER MINT CITRUS (ETHYL ALCOHOL) LIQUID

NDC Code(s): 76751-111-01, 76751-111-02, 76751-111-03, 76751-311-01, view more
76751-311-02, 76751-311-03, 76751-411-01, 76751-411-02, 76751-411-03, 76751-511-01, 76751-511-02, 76751-511-03, 76751-611-01, 76751-611-02, 76751-611-03
• Packager: OLIKA INC.

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DIVALPROEX SODIUM TABLET, DELAYED RELEASE

NDC Code(s): 55111-529-01, 55111-529-05, 55111-529-30, 55111-529-78, view more
55111-529-79, 55111-530-01, 55111-530-05, 55111-530-30, 55111-530-78, 55111-530-79, 55111-531-01, 55111-531-05, 55111-531-30, 55111-531-78, 55111-531-79
• Packager: DR.REDDY'S LABORATORIES LIMITED

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DIVALPROEX SODIUM TABLET, DELAYED RELEASE

NDC Code(s): 0832-7122-11, 0832-7122-15, 0832-7123-01, 0832-7123-11, view more
0832-7123-15, 0832-7123-89, 0832-7124-01, 0832-7124-11, 0832-7124-15, 0832-7124-89
• Packager: UPSHER-SMITH LABORATORIES, LLC

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DIVALPROEX SODIUM TABLET, DELAYED RELEASE

NDC Code(s): 57237-047-01, 57237-047-05, 57237-048-01, 57237-048-05, view more
57237-106-01, 57237-106-05
• Packager: RISING PHARMA HOLDINGS, INC.