DailyMed - Search Results for INACTIVE_INGREDIENT:(polydextrose)

CARDIZEM LA (DILTIAZEM HYDROCHLORIDE) TABLET, EXTENDED RELEASE

NDC Code(s):

0187-2045-30, 0187-2045-90, 0187-2046-30, 0187-2046-90, view more

0187-2047-30, 0187-2047-90, 0187-2048-30, 0187-2048-90, 0187-2049-30, 0187-2049-90, 0187-2050-30, 0187-2050-90

Packager: BAUSCH HEALTH US LLC

DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE, AND AMPHETAMINE SULFATE) CAPSULE

NDC Code(s):

0115-1486-01, 0115-1487-01, 0115-1488-01, 0115-1489-01, view more

0115-1490-01, 0115-1491-01

Packager: AMNEAL PHARMACEUTICALS OF NEW YORK LLC

DILTIAZEM HYDROCHLORIDE (DILTIAZEM HYDROCHLORIDE EXTENDED-RELEASE TABLETS) TABLET, EXTENDED RELEASE

NDC Code(s):

68682-704-30, 68682-704-90, 68682-705-30, 68682-705-90, view more

68682-706-30, 68682-706-90, 68682-707-30, 68682-707-90, 68682-708-30, 68682-708-90, 68682-709-30, 68682-709-90

Packager: OCEANSIDE PHARMACEUTICALS

SIMVASTATIN TABLET

NDC Code(s):

21695-738-90, 21695-739-30, 21695-739-90, 21695-740-30, view more

21695-740-90, 21695-741-30, 21695-741-90, 21695-742-30, 21695-742-90

Packager: REBEL DISTRIBUTORS CORP
This is a repackaged label.
Source NDC Code(s): 16252-505, 16252-506, 16252-507, 16252-508, view more
16252-509

SIMVASTATIN TABLET

NDC Code(s):

54868-5627-0, 54868-5627-1, 54868-5627-2, 54868-5628-0, view more

54868-5628-1, 54868-5628-2, 54868-5629-0, 54868-5629-1, 54868-5629-2, 54868-5629-4, 54868-5630-0, 54868-5630-1, 54868-6066-0

Packager: PHYSICIANS TOTAL CARE, INC.
This is a repackaged label.
Source NDC Code(s): 16252-505, 16252-506, 16252-507, 16252-508, view more
16252-509

METOPROLOL TARTRATE TABLET, FILM COATED

NDC Code(s):

0378-0018-01, 0378-0018-05, 0378-0032-01, 0378-0032-10, view more

0378-0047-01, 0378-0047-10, 0378-4593-01, 0378-4594-01

Packager: MYLAN PHARMACEUTICALS INC.

DILTIAZEM HYDROCHLORIDE CAPSULE, EXTENDED RELEASE

NDC Code(s):

50742-248-05, 50742-248-10, 50742-248-30, 50742-248-90, view more

50742-249-05, 50742-249-10, 50742-249-30, 50742-249-90, 50742-250-05, 50742-250-10, 50742-250-30, 50742-250-90, 50742-251-05, 50742-251-10, 50742-251-30, 50742-251-90, 50742-252-05, 50742-252-10, 50742-252-30, 50742-252-90

Packager: INGENUS PHARMACEUTICALS, LLC

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.

MEDIQUE IPRIN (IBUPROFEN) TABLET, FILM COATED DOVER ADDAPRIN (IBUPROFEN) TABLET, FILM COATED MEDI-FIRST IBUPROFEN (IBUPROFEN) TABLET, FILM COATED MEDI-FIRST PLUS IBUPROFEN (IBUPROFEN) TABLET, FILM COATED OTIS CLAPP ULTRAPRIN (IBUPROFEN) TABLET, FILM COATED

NDC Code(s):

47682-600-13, 47682-600-47, 47682-600-64, 47682-600-69, view more

47682-600-99, 47682-602-13, 47682-602-99, 47682-608-13, 47682-608-30, 47682-608-33, 47682-608-48, 47682-608-50, 47682-608-99, 47682-609-13, 47682-609-33, 47682-609-48, 47682-614-13, 47682-614-99

Packager: UNIFIRST FIRST AID CORPORATION

ADVIL PM- DIPHENHYDRAMINE CITRATE AND IBUPROFEN TABLET, COATED (ADVIL PM) TABLET, COATED

NDC Code(s):

29485-6533-4, 29485-6644-2, 29485-7008-3, 29485-7088-4, view more

29485-7937-6

Packager: LIL DRUG STORE PRODUCTS, INC

PAROXETINE (PAROXETINE HYDROCHLORIDE HEMIHYDRATE) TABLET, FILM COATED

NDC Code(s):

53808-0393-1, 53808-0394-1, 53808-0601-1, 53808-0655-1

Packager: STATE OF FLORIDA DOH CENTRAL PHARMACY
This is a repackaged label.
Source NDC Code(s): 0378-7001, 0378-7002, 0378-7003, 0378-7004

RISPERIDONE TABLET, FILM COATED

NDC Code(s):

43353-754-15, 43353-754-16, 43353-754-30, 43353-754-45, view more

43353-754-60, 43353-755-15, 43353-755-30, 43353-755-45, 43353-755-60, 43353-757-15, 43353-757-30, 43353-757-45, 43353-766-30

Packager: APHENA PHARMA SOLUTIONS - TENNESSEE, LLC
This is a repackaged label.
Source NDC Code(s): 0378-3511, 0378-3512, 0378-3513, 0378-3514

CARVEDILOL TABLET, FILM COATED

NDC Code(s):

43353-132-53, 43353-132-60, 43353-133-30, 43353-133-53, view more

43353-133-60, 43353-133-80, 43353-156-53, 43353-156-60, 43353-156-80, 43353-160-30, 43353-160-53, 43353-160-60, 43353-160-70, 43353-160-80

Packager: APHENA PHARMA SOLUTIONS - TENNESSEE, LLC
This is a repackaged label.
Source NDC Code(s): 0378-3631, 0378-3632, 0378-3633, 0378-3634

CARVEDILOL TABLET, FILM COATED

NDC Code(s):

51079-771-01, 51079-771-20, 51079-930-01, 51079-930-20, view more

51079-931-01, 51079-931-20, 51079-932-01, 51079-932-20

Packager: MYLAN INSTITUTIONAL INC.
This is a repackaged label.
Source NDC Code(s): 0378-3631, 0378-3632, 0378-3633, 0378-3634

CARVEDILOL TABLET, FILM COATED

NDC Code(s):

55154-5675-0, 55154-5676-0, 55154-5677-0, 55154-5678-0

Packager: CARDINAL HEALTH 107, LLC
This is a repackaged label.
Source NDC Code(s): 51079-771, 51079-930, 51079-931, 51079-932

BENAZEPRIL HYDROCHLORIDE TABLET, COATED

NDC Code(s):

51407-462-01, 51407-462-05, 51407-463-01, 51407-463-05, view more

51407-464-01, 51407-464-05, 51407-465-01, 51407-465-05

Packager: GOLDEN STATE MEDICAL SUPPLY, INC.
This is a repackaged label.
Source NDC Code(s): 43547-335, 43547-336, 43547-337, 43547-338

METOPROLOL SUCCINATE TABLET, EXTENDED RELEASE

NDC Code(s):

51407-403-01, 51407-403-10, 51407-404-01, 51407-404-10, view more

51407-405-01, 51407-405-10, 51407-406-01, 51407-406-08, 51407-406-10

Packager: GOLDEN STATE MEDICAL SUPPLY, INC.
This is a repackaged label.
Source NDC Code(s): 50742-615, 50742-616, 50742-617, 50742-618

PAROXETINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s):

69584-671-03, 69584-671-09, 69584-671-10, 69584-671-50, view more

69584-671-90, 69584-672-03, 69584-672-09, 69584-672-10, 69584-672-50, 69584-672-90, 69584-673-03, 69584-673-09, 69584-673-10, 69584-673-50, 69584-673-90, 69584-674-03, 69584-674-09, 69584-674-10, 69584-674-50, 69584-674-90

Packager: OXFORD PHARMACEUTICALS, LLC

TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED

NDC Code(s):

51079-572-01, 51079-572-20, 51079-573-01, 51079-573-20, view more

51079-574-01, 51079-574-20, 51079-575-01, 51079-575-20

Packager: MYLAN INSTITUTIONAL INC.
This is a repackaged label.
Source NDC Code(s): 0378-2401, 0378-2402, 0378-2405, 0378-2410

NISOLDIPINE TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s):

0677-1978-01, 0677-1979-01, 0677-1980-01, 0677-1981-01

Packager: UNITED RESEARCH LABORATORIES, INC.

SEARCH RESULTS for: INACTIVE_INGREDIENT:(polydextrose) (1000 results) Only the first 1000 of 1412 Advanced Search results were returned, please refine your search further by modifying your query.

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SEARCH RESULTS for: INACTIVE_INGREDIENT:(polydextrose) (1000 results)
Only the first 1000 of 1412 Advanced Search results were returned, please refine your search further by modifying your query.