NDC 65862-673

Felodipine

Felodipine

Felodipine 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 Felodipine.

Product ID65862-673_26026adc-6811-4eb1-9a0d-b7ad05d14d95
NDC65862-673
Product TypeHuman Prescription Drug
Proprietary NameFelodipine
Generic NameFelodipine
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2013-01-17
Marketing CategoryANDA / DRUG FOR FURTHER PROCESSING
Application NumberANDA203417
Labeler NameAurobindo Pharma Limited
Substance NameFELODIPINE
Active Ingredient Strength3 mg/1
Pharm ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 65862-673-01

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-673-01)
Marketing Start Date2013-01-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 65862-673-10 [65862067310]

Felodipine TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203417
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-01-17

NDC 65862-673-78 [65862067378]

Felodipine TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203417
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-01-17

NDC 65862-673-99 [65862067399]

Felodipine TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203417
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-01-17

NDC 65862-673-90 [65862067390]

Felodipine TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203417
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-01-17

NDC 65862-673-01 [65862067301]

Felodipine TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203417
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-01-17

Drug Details

Active Ingredients

IngredientStrength
FELODIPINE2.5 mg/1

Medicade Reported Pricing

65862067301 FELODIPINE ER 2.5 MG TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Felodipine" or generic name "Felodipine"

NDCBrand NameGeneric Name
0378-5011FelodipineFelodipine
0378-5012FelodipineFelodipine
0378-5013FelodipineFelodipine
0603-3581FelodipineFelodipine
0603-3582FelodipineFelodipine
0603-3583FelodipineFelodipine
0615-6572FelodipineFelodipine
0615-6573FelodipineFelodipine
13668-132FelodipineFelodipine
13668-133FelodipineFelodipine
13668-134FelodipineFelodipine
23155-048FelodipineFelodipine
23155-049FelodipineFelodipine
23155-050FelodipineFelodipine
45865-445FelodipineFelodipine
45865-446FelodipineFelodipine
50090-1125FelodipineFelodipine
50090-2421FelodipineFelodipine
50090-4808FelodipineFelodipine Extended-release Tablets
50090-5870FelodipineFelodipine
51079-467FelodipineFelodipine
51407-087FelodipineFelodipine
51407-088FelodipineFelodipine
51407-089FelodipineFelodipine
68071-4466FelodipineFelodipine
68151-3083FelodipineFelodipine
68151-3084FelodipineFelodipine
68462-235FelodipineFelodipine
68462-233FelodipineFelodipine
68462-234FelodipineFelodipine
69117-0029FelodipineFelodipine
69117-0030FelodipineFelodipine
69117-0028FelodipineFelodipine
53489-368FelodipineFelodipine
53489-369FelodipineFelodipine
53489-370FelodipineFelodipine
55289-306FelodipineFelodipine
55648-412FELODIPINEFELODIPINE
55648-414FELODIPINEFELODIPINE
55648-411FELODIPINEFELODIPINE
57237-110FelodipineFelodipine
57237-108FelodipineFelodipine
57237-109FelodipineFelodipine
59746-370FelodipineFelodipine
59746-369FelodipineFelodipine
59746-371FelodipineFelodipine
63629-5418FelodipineFelodipine
64679-411FELODIPINEFELODIPINE
64679-414FELODIPINEFELODIPINE
64679-412FELODIPINEFELODIPINE
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