SEARCH RESULTS for: 1000001 [RxCUI] (10 results)

• 

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

NDC Code(s): 31722-892-30, 31722-892-31, 31722-892-32, 31722-892-90, view more
31722-893-30, 31722-893-31, 31722-893-32, 31722-893-90, 31722-894-30, 31722-894-31, 31722-894-32, 31722-894-90, 31722-895-30, 31722-895-31, 31722-895-32, 31722-895-90, 31722-896-30, 31722-896-31, 31722-896-32, 31722-896-90
• Packager: Camber Pharmaceuticals, Inc.

• 

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

NDC Code(s): 42571-245-05, 42571-245-10, 42571-245-30, 42571-245-90, view more
42571-246-05, 42571-246-10, 42571-246-30, 42571-246-90, 42571-247-05, 42571-247-10, 42571-247-30, 42571-247-90, 42571-248-05, 42571-248-10, 42571-248-30, 42571-248-90, 42571-249-05, 42571-249-10, 42571-249-30, 42571-249-90
• Packager: Micro Labs Limited

• 

OLMESARTAN MEDOXOMIL AMLODIPINE AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 33342-243-07, 33342-243-10, 33342-244-07, 33342-244-10, view more
33342-245-07, 33342-245-10, 33342-246-07, 33342-246-10, 33342-247-07, 33342-247-10
• Packager: Macleods Pharmaceuticals Limited

• 

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.

• 

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

• 

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

• 

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 Health USA, LLC

• 

OLMESARTAN MEDOXOMIL / AMLODIPINE BESYLATE / HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 70518-4165-0
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 49884-788

• 

OLMESARTAN MEDOXOMIL AND AMLODIPINE BESYLATE AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 70436-014-04, 70436-014-06, 70436-015-04, 70436-015-06, view more
70436-016-04, 70436-016-06, 70436-017-04, 70436-017-06, 70436-018-04, 70436-018-06
• Packager: Slate Run Pharmaceuticals, LLC

• 

TRIBENZOR (olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide) tablet, film coated

NDC Code(s): 0713-0874-30, 0713-0875-30, 0713-0876-30, 0713-0877-30, view more
0713-0878-30
• Packager: Cosette Pharmaceuticals, Inc.