NDC 65862-249

Alfuzosin Hydrochloride

Alfuzosin Hydrochloride

Alfuzosin Hydrochloride is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is Alfuzosin Hydrochloride.

Product ID65862-249_15bdc59b-0888-4925-8d7b-8fb4c7673d05
NDC65862-249
Product TypeHuman Prescription Drug
Proprietary NameAlfuzosin Hydrochloride
Generic NameAlfuzosin Hydrochloride
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2012-08-30
Marketing CategoryANDA / DRUG FOR FURTHER PROCESSING
Application NumberANDA079060
Labeler NameAurobindo Pharma Limited
Substance NameALFUZOSIN HYDROCHLORIDE
Active Ingredient Strength10 mg/1
Pharm ClassesAdrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 65862-249-01

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-249-01)
Marketing Start Date2012-08-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65862-249-90 [65862024990]

Alfuzosin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA079060
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-08-30

NDC 65862-249-99 [65862024999]

Alfuzosin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA079060
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-08-30

NDC 65862-249-30 [65862024930]

Alfuzosin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA079060
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-08-30

NDC 65862-249-05 [65862024905]

Alfuzosin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA079060
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-08-30

NDC 65862-249-01 [65862024901]

Alfuzosin Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA079060
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-08-30

Drug Details

Active Ingredients

IngredientStrength
ALFUZOSIN HYDROCHLORIDE10 mg/1

Medicade Reported Pricing

65862024901 ALFUZOSIN HCL ER 10 MG TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Alfuzosin Hydrochloride" or generic name "Alfuzosin Hydrochloride"

NDCBrand NameGeneric Name
0378-5005Alfuzosin Hydrochloridealfuzosin
0440-5000Alfuzosin hydrochlorideAlfuzosin hydrochloride
13668-021ALFUZOSIN HYDROCHLORIDEALFUZOSIN HYDROCHLORIDE
29300-155Alfuzosin hydrochlorideAlfuzosin hydrochloride
31722-302Alfuzosin HydrochlorideAlfuzosin Hydrochloride
33261-994Alfuzosin HydrochlorideAlfuzosin Hydrochloride
42291-110Alfuzosin HydrochlorideAlfuzosin Hydrochloride
43353-746Alfuzosin Hydrochloridealfuzosin
43353-945Alfuzosin hydrochlorideAlfuzosin hydrochloride
47335-956Alfuzosin HydrochlorideAlfuzosin Hydrochloride
55648-738Alfuzosin HydrochlorideAlfuzosin Hydrochloride
57237-114Alfuzosin HydrochlorideAlfuzosin Hydrochloride
60505-2850Alfuzosin HydrochlorideAlfuzosin Hydrochloride
61919-349ALFUZOSIN HYDROCHLORIDEALFUZOSIN HYDROCHLORIDE
63629-2353Alfuzosin HydrochlorideAlfuzosin Hydrochloride
63629-2354Alfuzosin HydrochlorideAlfuzosin Hydrochloride
63629-7907Alfuzosin hydrochlorideAlfuzosin hydrochloride
63629-9155Alfuzosin hydrochlorideAlfuzosin hydrochloride
63629-9295Alfuzosin HydrochlorideAlfuzosin Hydrochloride
64679-738Alfuzosin HydrochlorideAlfuzosin Hydrochloride
65862-249Alfuzosin HydrochlorideAlfuzosin Hydrochloride
69097-844Alfuzosin HydrochlorideAlfuzosin Hydrochloride
70934-306Alfuzosin HydrochlorideAlfuzosin Hydrochloride
70934-961Alfuzosin HydrochlorideAlfuzosin Hydrochloride
76282-302Alfuzosin hydrochlorideAlfuzosin hydrochloride
71335-1529Alfuzosin HydrochlorideAlfuzosin Hydrochloride
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.