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Procardia XL - 0069-2650-41 - (nifedipine)

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Drug Information of Procardia XL

Product NDC: 0069-2650
Proprietary Name: Procardia XL
Non Proprietary Name: nifedipine
Active Ingredient(s): 30    mg/1 & nbsp;   nifedipine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Procardia XL

Product NDC: 0069-2650
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019684
Marketing Category: NDA
Start Marketing Date: 19890906

Package Information of Procardia XL

Package NDC: 0069-2650-41
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0069-2650-41)

NDC Information of Procardia XL

NDC Code 0069-2650-41
Proprietary Name Procardia XL
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0069-2650-41)
Product NDC 0069-2650
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nifedipine
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19890906
Marketing Category Name NDA
Labeler Name Pfizer Laboratories Div Pfizer Inc
Substance Name NIFEDIPINE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Procardia XL


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