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Theophylline(Anhydrous) - 16571-011-01 - (Theophylline)

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Drug Information of Theophylline(Anhydrous)

Product NDC: 16571-011
Proprietary Name: Theophylline(Anhydrous)
Non Proprietary Name: Theophylline
Active Ingredient(s): 400    mg/1 & nbsp;   Theophylline
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Theophylline(Anhydrous)

Product NDC: 16571-011
Labeler Name: PACK Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040595
Marketing Category: ANDA
Start Marketing Date: 20100915

Package Information of Theophylline(Anhydrous)

Package NDC: 16571-011-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-011-01)

NDC Information of Theophylline(Anhydrous)

NDC Code 16571-011-01
Proprietary Name Theophylline(Anhydrous)
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-011-01)
Product NDC 16571-011
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Theophylline
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100915
Marketing Category Name ANDA
Labeler Name PACK Pharmaceuticals, LLC
Substance Name THEOPHYLLINE ANHYDROUS
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Methylxanthine [EPC],Xanthines [Chemical/Ingredient]

Complete Information of Theophylline(Anhydrous)


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