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