NDC 0093-2068

Doxazosin

Doxazosin Mesylate

Doxazosin is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Teva Pharmaceuticals Usa, Inc.. The primary component is Doxazosin Mesylate.

• Product ID: 0093-2068_1147fddf-c4b3-405b-8509-57480349362f
• NDC: 0093-2068
• Product Type: Human Prescription Drug
• Proprietary Name: Doxazosin
• Generic Name: Doxazosin Mesylate
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2014-09-09
• Marketing Category: ANDA / ANDA
• Application Number: ANDA075536
• Labeler Name: Teva Pharmaceuticals USA, Inc.
• Substance Name: DOXAZOSIN MESYLATE
• Active Ingredient Strength: 4 mg/1
• Pharm Classes: Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0093-2068-01

100 TABLET in 1 BOTTLE (0093-2068-01)

• Marketing Start Date: 2014-09-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0093-2068-05 [00093206805]

Doxazosin TABLET

• Marketing Category: ANDA
• Application Number: ANDA075536
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-09-09
• Marketing End Date: 2014-09-09

NDC 0093-2068-01 [00093206801]

Doxazosin TABLET

• Marketing Category: ANDA
• Application Number: ANDA075536
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2014-09-12

NDC 0093-2068-93 [00093206893]

Doxazosin TABLET

• Marketing Category: ANDA
• Application Number: ANDA075536
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-09-09
• Marketing End Date: 2014-09-09

NDC 0093-2068-19 [00093206819]

Doxazosin TABLET

• Marketing Category: ANDA
• Application Number: ANDA075536
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-09-09
• Marketing End Date: 2019-12-09

Drug Details

Active Ingredients

Ingredient	Strength
DOXAZOSIN MESYLATE	4 mg/1

OpenFDA Data

• SPL SET ID: 0aaa68a7-f73b-46d8-860f-a76d96897489
• Manufacturer:
  • Teva Pharmaceuticals USA, Inc.
• UNII:
  • 86P6PQK0MU
• RxNorm Concept Unique ID - RxCUI:
  • 197628
  • 197625
  • 197627
  • 197626
• UPC Code:
  • 0300932070011
  • 0300932069015
  • 0300932068018
  • 0300932067011

Pharmacological Class

• Adrenergic alpha-Antagonists [MoA]
• alpha-Adrenergic Blocker [EPC]

NDC Crossover Matching brand name "Doxazosin" or generic name "Doxazosin Mesylate"

NDC	Brand Name	Generic Name
68071-1889	Doxazosin	Doxazosin
68071-4273	Doxazosin	Doxazosin
68071-3298	Doxazosin	Doxazosin
68071-3331	Doxazosin	Doxazosin
68071-3341	Doxazosin	Doxazosin
68071-4272	Doxazosin	Doxazosin
68084-862	Doxazosin	Doxazosin
68084-836	Doxazosin	Doxazosin
68084-851	Doxazosin	Doxazosin
68382-783	Doxazosin	Doxazosin
68382-785	Doxazosin	Doxazosin
68382-784	Doxazosin	Doxazosin
68382-786	Doxazosin	Doxazosin
68645-464	Doxazosin	Doxazosin
68645-465	Doxazosin	Doxazosin
68645-463	Doxazosin	Doxazosin
68788-7149	Doxazosin	Doxazosin
68788-7328	Doxazosin	Doxazosin
68788-9675	Doxazosin	Doxazosin
70518-0839	Doxazosin	Doxazosin
70518-1061	Doxazosin	Doxazosin
70518-1645	Doxazosin	Doxazosin
70518-1560	Doxazosin	Doxazosin
70518-1804	Doxazosin	Doxazosin
70771-1115	Doxazosin	Doxazosin
70771-1114	Doxazosin	Doxazosin
70771-1112	Doxazosin	Doxazosin
70771-1113	Doxazosin	Doxazosin
71335-0309	Doxazosin	Doxazosin
71335-0349	Doxazosin	Doxazosin
71335-0002	Doxazosin	Doxazosin
71610-153	Doxazosin	Doxazosin
0615-5536	Doxazosin	Doxazosin
0615-6570	Doxazosin	Doxazosin
0615-6571	Doxazosin	Doxazosin
71610-160	Doxazosin	Doxazosin
0615-5537	Doxazosin	Doxazosin
71610-043	Doxazosin	Doxazosin
0832-0357	Doxazosin	Doxazosin
0832-0356	Doxazosin	Doxazosin
0832-1359	Doxazosin	Doxazosin
0832-1358	Doxazosin	Doxazosin
0904-5523	Doxazosin	Doxazosin
0904-5524	Doxazosin	Doxazosin
0904-5522	Doxazosin	Doxazosin
0093-2067	Doxazosin	Doxazosin
0093-2068	Doxazosin	Doxazosin
0093-2069	Doxazosin	Doxazosin
0093-2070	Doxazosin	Doxazosin
16729-211	Doxazosin	Doxazosin