DailyMed - Search Results for INACTIVE_INGREDIENT:(acrylates copolymer)

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 (TITANIUM DIOXIDE AND ZINC OXIDE) SUSPENSION

NDC Code(s):

70186-580-01, 70186-581-01, 70186-582-01, 70186-583-01, view more

70186-584-01, 70186-585-01, 70186-586-01, 70186-587-01, 70186-588-01, 70186-589-01, 70186-590-01, 70186-591-01, 70186-592-01, 70186-593-01, 70186-594-01, 70186-595-01, 70186-596-01, 70186-597-01, 70186-598-01, 70186-599-01

Packager: CHARLOTTE TILBURY BEAUTY LTD.

DEXMETHYLPHENIDATE HYDROCHLORIDE EXTENDED-RELEASE (DEXMETHYLPHENIDATE HYDROCHLORIDE) CAPSULE, EXTENDED RELEASE

NDC Code(s):

0527-8106-37, 0527-8107-37, 0527-8108-37, 0527-8109-37, view more

0527-8110-37, 0527-8111-37, 0527-8112-37, 0527-8113-37

Packager: LANNETT COMPANY, INC.

DEXMETHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE

NDC Code(s):

49884-048-01, 49884-049-01, 49884-090-01, 49884-248-01, view more

49884-333-01, 49884-339-01, 49884-539-01, 49884-546-01

Packager: PAR PHARMACEUTICAL, INC.

APTENSIO XR (METHYLPHENIDATE HYDROCHLORIDE) CAPSULE, EXTENDED RELEASE

NDC Code(s):

42858-401-45, 42858-402-45, 42858-403-45, 42858-404-45, view more

42858-405-45, 42858-406-45, 42858-407-45

Packager: RHODES PHARMACEUTICALS L.P.

METHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE

NDC Code(s):

42858-075-45, 42858-076-45, 42858-077-45, 42858-078-45, view more

42858-079-45, 42858-080-45, 42858-081-45

Packager: RHODES PHARMACEUTICALS

METHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE

NDC Code(s):

0591-3854-19, 0591-3862-19, 0591-3869-19, 0591-3873-19, view more

0591-3891-19, 0591-3895-19, 0591-3902-19

Packager: ACTAVIS PHARMA, INC.

MORPHINE SULFATE CAPSULE, EXTENDED RELEASE

NDC Code(s):

0115-1277-01, 0115-1277-03, 0115-1277-08, 0115-1278-01, view more

0115-1278-03, 0115-1278-08, 0115-1279-01, 0115-1279-03, 0115-1279-08, 0115-1280-01, 0115-1280-03, 0115-1280-08, 0115-1281-01, 0115-1281-03, 0115-1281-08, 0115-1282-01, 0115-1282-03, 0115-1282-08, 0115-1479-01

Packager: AMNEAL PHARMACEUTICALS OF NEW YORK LLC

MORPHINE SULFATE CAPSULE, EXTENDED RELEASE

NDC Code(s):

0832-0225-00, 0832-0225-50, 0832-0226-00, 0832-0226-50, view more

0832-0227-00, 0832-0227-50, 0832-0228-00, 0832-0228-50, 0832-0229-00, 0832-0229-50, 0832-0230-00, 0832-0230-50, 0832-0233-00, 0832-0233-50

Packager: UPSHER-SMITH LABORATORIES, LLC

DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE, AMPHETAMINE SULFATE EXTENDED-RELEASE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE, AMPHETAMINE SULFATE) CAPSULE, EXTENDED RELEASE

NDC Code(s):

57664-336-88, 57664-337-88, 57664-338-88, 57664-339-88, view more

57664-340-88, 57664-341-88

Packager: SUN PHARMACEUTICAL INDUSTRIES, INC.

LAMOTRIGINE TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s):

42291-443-30, 42291-444-30, 42291-445-30, 42291-446-30, view more

42291-447-30, 42291-448-30

Packager: AVKARE
This is a repackaged label.
Source NDC Code(s): 65162-949, 65162-956, 65162-958, 65162-986, view more
65162-988, 65162-990

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

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.

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.

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

NDC Code(s):

51407-557-01, 51407-558-01, 51407-559-01, 51407-560-01, view more

51407-561-01, 51407-562-01

Packager: GOLDEN STATE MEDICAL SUPPLY, INC.

LAMOTRIGINE (LAMOTRIGINE EXTENDED-RELEASE) TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s):

31722-240-30, 31722-241-30, 31722-242-30, 31722-243-30, view more

31722-244-30, 31722-245-30

Packager: CAMBER PHARMACEUTICALS INC

PAROXETINE HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE

NDC Code(s):

60505-1316-3, 60505-1317-3, 60505-1318-3, 60505-3673-3, view more

60505-3674-3, 60505-3675-3

Packager: APOTEX CORP

LAMOTRIGINE TABLET, EXTENDED RELEASE

NDC Code(s):

16714-623-01, 16714-624-01, 16714-625-01, 16714-626-01, view more

16714-627-01, 16714-893-01

Packager: NORTHSTAR RX LLC

LAMOTRIGINE TABLET, EXTENDED RELEASE

NDC Code(s):

68382-979-05, 68382-979-06, 68382-979-16, 68382-980-05, view more

68382-980-06, 68382-980-16, 68382-981-05, 68382-981-06, 68382-981-16, 68382-982-05, 68382-982-06, 68382-982-16, 68382-983-05, 68382-983-06, 68382-983-16, 68382-984-05, 68382-984-06, 68382-984-16

Packager: ZYDUS PHARMACEUTICALS USA INC.

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

NDC Code(s):

43975-277-10, 43975-278-10, 43975-279-10, 43975-280-10, view more

43975-281-10, 43975-282-10

Packager: ANI PHARMACEUTICALS, INC.

PROTECT U GUARD 63% FOAMING HAND SANITIZER LEMON (ETHYL ALCOHOL) LIQUID PROTECT U GUARD 63% FOAMING HAND SANITIZER LAVENDER (ETHYL ALCOHOL) LIQUID PROTECT U GUARD 63% FOAMING HAND SANITIZER COTTON (ETHYL ALCOHOL) LIQUID PROTECT U GUARD 63% FOAMING HAND SANITIZER (ETHYL ALCOHOL) LIQUID PROTECT U GUARD 63% FOAMING HAND SANITIZER WATERMELON (ETHYL ALCOHOL) LIQUID PROTECT U GUARD 63% FOAMING HAND SANITIZER FRESH (ETHYL ALCOHOL) LIQUID

NDC Code(s):

71788-010-10, 71788-010-20, 71788-010-50, 71788-010-60, view more

71788-010-70, 71788-010-80, 71788-011-10, 71788-011-20, 71788-011-50, 71788-011-60, 71788-011-70, 71788-011-80, 71788-012-10, 71788-012-20, 71788-012-50, 71788-012-60, 71788-012-70, 71788-012-80, 71788-013-10, 71788-013-20, 71788-013-50, 71788-013-60, 71788-013-70, 71788-013-80, 71788-014-10, 71788-014-20, 71788-014-50, 71788-014-60, 71788-014-70, 71788-014-80, 71788-015-10, 71788-015-20, 71788-015-50, 71788-015-60, 71788-015-70, 71788-015-80

Packager: PROTECT U GUARD, LLC

SEARCH RESULTS for: INACTIVE_INGREDIENT:(acrylates copolymer) (1000 results) Only the first 1000 of 3415 Advanced Search results were returned, please refine your search further by modifying your query.

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SEARCH RESULTS for: INACTIVE_INGREDIENT:(acrylates copolymer) (1000 results)
Only the first 1000 of 3415 Advanced Search results were returned, please refine your search further by modifying your query.