SEARCH RESULTS for: hydrochlorothiazide; olmesartan medoxomil (47 results)

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OLMESARTAN MEDOXOMIL, AMLODIPINE AND HYDROCHLOROTHIAZIDE 20/5/12.5 MG (olmesartan medoxomil, amlodipine and hydrochlorothiazide tablet 20/5/12.5 mg) tablet
OLMESARTAN MEDOXOMIL, AMLODIPINE AND HYDROCHLOROTHIAZIDE 40/5/12.5 MG (olmesartan medoxomil, amlodipine and hydrochlorothiazide tablet 40/5/12.5 mg) tablet
OLMESARTAN MEDOXOMIL, AMLODIPINE AND HYDROCHLOROTHIAZIDE 40/5/25 MG (olmesartan medoxomil, amlodipine and hydrochlorothiazide tablet 40/5/25 mg) tablet
OLMESARTAN MEDOXOMIL, AMLODIPINE AND HYDROCHLOROTHIAZIDE 40/10/12.5 MG (olmesartan medoxomil, amlodipine and hydrochlorothiazide tablet 40/10/12.5 mg) tablet
OLMESARTAN MEDOXOMIL, AMLODIPINE AND HYDROCHLOROTHIAZIDE 40/10/25 MG (olmesartan medoxomil, amlodipine and hydrochlorothiazide tablet 40/10/25 mg) tablet

NDC Code(s): 13668-382-05, 13668-382-30, 13668-382-90, 13668-383-05, view more
13668-383-30, 13668-383-90, 13668-385-05, 13668-385-30, 13668-385-90, 13668-386-05, 13668-386-30, 13668-386-90, 13668-397-05, 13668-397-30, 13668-397-90
• Packager: Torrent Pharmaceuticals Limited

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OLMESARTAN MEDOXOMIL, AMLODIPINE AND HYDROCHLOROTHIAZIDE (olmesartan medoxomil, amlodipine besylate and hydrochlorothiazide) tablet, film coated

NDC Code(s): 57664-796-83, 57664-796-99, 57664-797-83, 57664-797-99, view more
57664-798-83, 57664-798-99, 57664-799-83, 57664-799-99, 57664-800-83, 57664-800-99
• Packager: Sun Pharmaceutical Industries, Inc.

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OLMESARTAN MEDOXOMIL, AMLODIPINE AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 0093-5002-56, 0093-5003-56, 0093-5004-56, 0093-5005-56, view more
0093-5006-56
• Packager: Teva Pharmaceuticals USA, Inc.

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OLMESARTAN MEDOXOMIL / AMLODIPINE BESYLATE / HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 49884-786-09, 49884-786-11, 49884-787-09, 49884-787-11, view more
49884-788-09, 49884-788-11, 49884-789-09, 49884-789-11, 49884-790-09, 49884-790-11
• Packager: Par Pharmaceutical, Inc.

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OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE (olmesartan medoxomil and hydrochlorothiazide) tablet

NDC Code(s): 70756-812-12, 70756-812-30, 70756-812-51, 70756-812-90, view more
70756-813-12, 70756-813-30, 70756-813-51, 70756-813-90, 70756-814-12, 70756-814-30, 70756-814-51, 70756-814-90
• Packager: Lifestar Pharma LLC

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OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 62332-149-08, 62332-149-10, 62332-149-30, 62332-149-90, view more
62332-149-91, 62332-150-08, 62332-150-10, 62332-150-30, 62332-150-90, 62332-150-91, 62332-151-08, 62332-151-10, 62332-151-30, 62332-151-90, 62332-151-91
• Packager: Alembic Pharmaceuticals Inc.

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OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 46708-149-08, 46708-149-10, 46708-149-30, 46708-149-90, view more
46708-149-91, 46708-150-08, 46708-150-10, 46708-150-30, 46708-150-90, 46708-150-91, 46708-151-08, 46708-151-10, 46708-151-30, 46708-151-90, 46708-151-91
• Packager: Alembic Pharmaceuticals Limited

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OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 16729-366-10, 16729-366-15, 16729-366-16, 16729-366-17, view more
16729-366-45, 16729-366-46, 16729-367-10, 16729-367-15, 16729-367-16, 16729-367-17, 16729-367-45, 16729-367-46, 16729-368-10, 16729-368-15, 16729-368-16, 16729-368-17, 16729-368-45, 16729-368-46
• Packager: Accord Healthcare Inc.

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OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 65862-779-10, 65862-779-30, 65862-779-78, 65862-779-90, view more
65862-779-99, 65862-780-10, 65862-780-30, 65862-780-78, 65862-780-90, 65862-780-99, 65862-781-10, 65862-781-30, 65862-781-78, 65862-781-90, 65862-781-99
• Packager: Aurobindo Pharma Limited

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OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 33342-173-07, 33342-173-10, 33342-173-12, 33342-173-44, view more
33342-174-07, 33342-174-10, 33342-174-12, 33342-174-44, 33342-175-07, 33342-175-10, 33342-175-12, 33342-175-44
• Packager: Macleods Pharmaceuticals Limited

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OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 43547-391-03, 43547-391-09, 43547-391-11, 43547-392-03, view more
43547-392-09, 43547-392-11, 43547-393-03, 43547-393-09, 43547-393-11
• Packager: Solco Healthcare US, LLC

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OLMESARTAN MEDOXOMIL, AMLODIPINE AND HYDROCHLOROTHIAZIDE (olmesartan medoxomil, amlodipine besylate and hydrochlorothiazide) tablet, film coated

NDC Code(s): 53808-1120-1
• Packager: DOH CENTRAL PHARMACY
• This is a repackaged label.
• Source NDC Code(s): 57664-796

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OLMESARTAN MEDOXOMIL / AMLODIPINE BESYLATE / HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 63629-2238-1
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 49884-786

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OLMESARTAN MEDOXOMIL / AMLODIPINE BESYLATE / HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 72162-1515-3
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 49884-788

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OLMESARTAN MEDOXOMIL / AMLODIPINE BESYLATE / HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 72162-1514-3, 72162-1514-9
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 49884-786

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OLMESARTAN MEDOXOMIL / AMLODIPINE BESYLATE / HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 72162-1516-9
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 49884-789

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OLMESARTAN MEDOXOMIL / AMLODIPINE BESYLATE / HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 63629-2240-1
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 49884-789

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OLMESARTAN MEDOXOMIL / AMLODIPINE BESYLATE / HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 63629-2239-1
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 49884-786

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OLMESARTAN MEDOXOMIL / AMLODIPINE BESYLATE / HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 63629-2241-1
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 49884-788

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OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE (olmesartan medoxomil and hydrochlorothiazide) tablet

NDC Code(s): 50090-6027-0, 50090-6027-1
• Packager: A-S Medication Solutions
• This is a repackaged label.
• Source NDC Code(s): 70756-812