NDC 13668-161

telmisartan and hydrochlorthiazide

Telmisartan And Hydrochlorthiazide

telmisartan and hydrochlorthiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Torrent Pharmaceuticals Limited. The primary component is Telmisartan; Hydrochlorothiazide.

• Product ID: 13668-161_06fdda4e-efb7-4c81-91b8-6fc648bd21da
• NDC: 13668-161
• Product Type: Human Prescription Drug
• Proprietary Name: telmisartan and hydrochlorthiazide
• Generic Name: Telmisartan And Hydrochlorthiazide
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2014-02-25
• Marketing Category: ANDA / ANDA
• Application Number: ANDA201192
• Labeler Name: Torrent Pharmaceuticals Limited
• Substance Name: TELMISARTAN; HYDROCHLOROTHIAZIDE
• Active Ingredient Strength: 80 mg/1; mg/1
• Pharm Classes: Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 13668-161-01

100 TABLET in 1 BOTTLE (13668-161-01)

• Marketing Start Date: 2014-02-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 13668-161-01 [13668016101]

telmisartan and hydrochlorthiazide TABLET

• Marketing Category: ANDA
• Application Number: ANDA201192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-02-25

NDC 13668-161-72 [13668016172]

telmisartan and hydrochlorthiazide TABLET

• Marketing Category: ANDA
• Application Number: ANDA201192
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2014-02-25

NDC 13668-161-30 [13668016130]

telmisartan and hydrochlorthiazide TABLET

• Marketing Category: ANDA
• Application Number: ANDA201192
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2014-02-25

NDC 13668-161-74 [13668016174]

telmisartan and hydrochlorthiazide TABLET

• Marketing Category: ANDA
• Application Number: ANDA201192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-02-25

Drug Details

Active Ingredients

Ingredient	Strength
TELMISARTAN	80 mg/1

OpenFDA Data

• SPL SET ID: 4ab13b8c-1110-477b-a6a3-ee93e33b9faa
• Manufacturer:
  • Torrent Pharmaceuticals Limited
• UNII:
  • U5SYW473RQ
  • 0J48LPH2TH
• RxNorm Concept Unique ID - RxCUI:
  • 477130
  • 283317
  • 283316
• UPC Code:
  • 0313668161014
  • 0313668160017
  • 0313668159011

Pharmacological Class

• Angiotensin 2 Receptor Antagonists [MoA]
• Angiotensin 2 Receptor Blocker [EPC]
• Increased Diuresis [PE]
• Thiazide Diuretic [EPC]
• Thiazides [CS]

Medicade Reported Pricing

13668016172 TELMISARTAN-HYDROCHLOROTHIAZIDE 80-25 MG TAB

Pricing Unit: EA | Drug Type:

13668016130 TELMISARTAN-HYDROCHLOROTHIAZIDE 80-25 MG TAB

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "telmisartan and hydrochlorthiazide" or generic name "Telmisartan And Hydrochlorthiazide"

NDC	Brand Name	Generic Name
13668-159	telmisartan and hydrochlorthiazide	telmisartan and hydrochlorthiazide
13668-160	telmisartan and hydrochlorthiazide	telmisartan and hydrochlorthiazide
13668-161	telmisartan and hydrochlorthiazide	telmisartan and hydrochlorthiazide