SEARCH RESULTS for: INACTIVE_INGREDIENT:(hypromellose 2910 (6 mpa.s)) (1000 results)
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QUETIAPINE FUMARATE TABLET, FILM COATED

NDC Code(s): 65862-489-01, 65862-489-10, 65862-489-99, 65862-490-01, view more
65862-490-10, 65862-490-99, 65862-491-01, 65862-491-10, 65862-491-99, 65862-492-01, 65862-492-10, 65862-492-99, 65862-493-01, 65862-493-10, 65862-493-99, 65862-494-01, 65862-494-10, 65862-494-60, 65862-494-99, 65862-495-01, 65862-495-05, 65862-495-10
• Packager: AUROBINDO PHARMA LIMITED

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DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE, AND AMPHETAMINE SULFATE CAPSULE, EXTENDED RELEASE

NDC Code(s): 51407-548-01, 51407-549-01, 51407-550-01, 51407-551-01, view more
51407-552-01, 51407-553-01
• Packager: GOLDEN STATE MEDICAL SUPPLY, INC.
• This is a repackaged label.
• Source NDC Code(s): 0527-5510, 0527-5511, 0527-5512, 0527-5513, view more
  0527-5514, 0527-5515

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DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE, AND AMPHETAMINE SULFATE CAPSULE, EXTENDED RELEASE

NDC Code(s): 64850-510-01, 64850-511-01, 64850-512-01, 64850-513-01, view more
64850-514-01, 64850-515-01
• Packager: ELITE LABORATORIES, INC.

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DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE CAPSULE, EXTENDED RELEASE

NDC Code(s): 70010-029-01, 70010-030-01, 70010-031-01, 70010-032-01, view more
70010-033-01, 70010-034-01
• Packager: GRANULES PHARMACEUTICALS INC.

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DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE, AND AMPHETAMINE SULFATE CAPSULE, EXTENDED RELEASE

NDC Code(s): 35573-464-02, 35573-465-02, 35573-466-02, 35573-467-02, view more
35573-468-02, 35573-469-02
• Packager: BUREL PHARMACEUTICALS, LLC

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PREMPHASE (CONJUGATED ESTROGENS AND MEDROXYPROGESTERONE ACETATE) KIT PREMPRO (CONJUGATED ESTROGENS AND MEDROXYPROGESTERONE ACETATE) TABLET, SUGAR COATED

NDC Code(s): 0046-1105-11, 0046-1106-11, 0046-1107-11, 0046-1108-11, view more
0046-2575-12
• Packager: WYETH PHARMACEUTICALS LLC, A SUBSIDIARY OF PFIZER INC.

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BREXPIPRAZOLE (BREXPIPRAZOLE) TABLET, FILM COATED

NDC Code(s): 31722-434-30, 31722-435-30, 31722-436-30, 31722-437-30, view more
31722-438-30, 31722-439-30
• Packager: CAMBER PHARMACEUTICALS, INC.

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OLANZAPINE TABLET, FILM COATED

NDC Code(s): 60429-620-10, 60429-620-30, 60429-621-10, 60429-621-30, view more
60429-622-10, 60429-622-30, 60429-623-10, 60429-623-30, 60429-624-10, 60429-624-30, 60429-625-10, 60429-625-30
• Packager: GOLDEN STATE MEDICAL SUPPLY, INC.
• This is a repackaged label.
• Source NDC Code(s): 60505-3110, 60505-3111, 60505-3112, 60505-3113, view more
  60505-3114, 60505-3140

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QUETIAPINE FUMARATE (QUETIAPINE) TABLET

NDC Code(s): 60687-327-01, 60687-327-11, 60687-338-01, 60687-338-11, view more
60687-349-01, 60687-349-11, 60687-360-01, 60687-360-11, 60687-371-01, 60687-371-11, 60687-382-01, 60687-382-11
• Packager: AMERICAN HEALTH PACKAGING
• This is a repackaged label.
• Source NDC Code(s): 68001-180, 68001-181, 68001-182, 68001-183, view more
  68001-184, 68001-185

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RISPERIDONE TABLET, FILM COATED

NDC Code(s): 13107-119-05, 13107-119-10, 13107-119-60, 13107-120-05, view more
13107-120-10, 13107-120-60, 13107-121-05, 13107-121-10, 13107-121-60, 13107-122-05, 13107-122-10, 13107-122-60, 13107-123-05, 13107-123-10, 13107-123-60, 13107-124-10, 13107-124-60
• Packager: AUROLIFE PHARMA LLC

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AMITRIPTYLINE HYDROCHLORIDE TABLET

NDC Code(s): 64330-630-01, 64330-631-01, 64330-632-01, 64330-633-01, view more
64330-634-01, 64330-635-01
• Packager: CENTAUR PHARMACEUTICALS PRIVATE LIMITED

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AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 70710-1225-0, 70710-1225-1, 70710-1226-0, 70710-1226-1, view more
70710-1227-0, 70710-1227-1, 70710-1228-0, 70710-1228-1, 70710-1229-0, 70710-1229-1, 70710-1230-0, 70710-1230-1
• Packager: ZYDUS PHARMACEUTICALS USA INC.

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OLANZAPINE TABLET

NDC Code(s): 67184-0561-1, 67184-0561-2, 67184-0561-3, 67184-0561-6, view more
67184-0562-1, 67184-0562-2, 67184-0562-3, 67184-0562-6, 67184-0563-1, 67184-0563-2, 67184-0563-4, 67184-0563-6, 67184-0564-1, 67184-0564-2, 67184-0564-5, 67184-0564-6, 67184-0565-1, 67184-0565-2, 67184-0565-4, 67184-0565-6, 67184-0566-1, 67184-0566-2, 67184-0566-5, 67184-0566-6
• Packager: QILU PHARMACEUTICAL CO., LTD.

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AMITRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 16714-257-01, 16714-257-02, 16714-258-01, 16714-258-02, view more
16714-259-01, 16714-259-02, 16714-260-01, 16714-261-01, 16714-262-01
• Packager: NORTHSTAR RX LLC.

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QUETIAPINE FUMARATE TABLET

NDC Code(s): 57297-445-01, 57297-445-03, 57297-445-13, 57297-446-01, view more
57297-446-03, 57297-446-13, 57297-447-01, 57297-447-03, 57297-447-13, 57297-448-01, 57297-448-02, 57297-448-03, 57297-448-13, 57297-449-01, 57297-449-02, 57297-449-03, 57297-449-07, 57297-449-13, 57297-450-01, 57297-450-02, 57297-450-03, 57297-450-13
• Packager: LUPIN LIMITED

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OLANZAPINE TABLET

NDC Code(s): 69543-380-30, 69543-380-90, 69543-381-30, 69543-381-90, view more
69543-382-30, 69543-382-90, 69543-383-30, 69543-383-90, 69543-384-30, 69543-384-90, 69543-385-30, 69543-385-90
• Packager: VIRTUS PHARMACEUTICALS, LLC

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OLANZAPINE TABLET

NDC Code(s): 72241-051-05, 72241-051-10, 72241-051-11, 72241-051-22, view more
72241-052-05, 72241-052-10, 72241-052-11, 72241-052-22, 72241-053-05, 72241-053-10, 72241-053-11, 72241-053-22, 72241-054-05, 72241-054-10, 72241-054-11, 72241-054-22, 72241-055-05, 72241-055-10, 72241-055-11, 72241-055-22, 72241-056-04, 72241-056-10, 72241-056-11, 72241-056-22
• Packager: MODAVAR PHARMACEUTICALS LLC

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AMITRIPTYLINE HYDROCHLORIDE TABLET

NDC Code(s): 69844-058-01, 69844-058-02, 69844-058-03, 69844-059-01, view more
69844-059-02, 69844-059-03, 69844-060-01, 69844-060-02, 69844-060-03, 69844-061-01, 69844-061-02, 69844-061-03, 69844-062-01, 69844-062-02, 69844-062-03, 69844-063-01, 69844-063-02, 69844-063-03
• Packager: GRAVITI PHARMACEUTICALS PRIVATE LIMITED

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PREMARIN (CONJUGATED ESTROGENS) TABLET, FILM COATED

NDC Code(s): 54868-0365-0, 54868-0365-2, 54868-0365-3, 54868-0451-2, view more
54868-0451-6, 54868-0453-0, 54868-0453-2, 54868-0453-4, 54868-0453-5, 54868-0453-6, 54868-2702-0, 54868-2702-1, 54868-4865-0, 54868-4865-1, 54868-4865-2, 54868-4865-3, 54868-4865-4
• Packager: PHYSICIANS TOTAL CARE, INC.
• This is a repackaged label.
• Source NDC Code(s): 0046-1100, 0046-1101, 0046-1102, 0046-1103, view more
  0046-1104

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CHLORPROMAZINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s): 0904-7129-61, 0904-7130-06, 0904-7130-61, 0904-7131-61, view more
0904-7132-61, 0904-7133-61
• Packager: MAJOR PHARMACEUTICALS
• This is a repackaged label.
• Source NDC Code(s): 70710-1129, 70710-1130, 70710-1131, 70710-1132, view more
  70710-1133