Home
>
National Drug Code (NDC)
>
Uniphyl
Uniphyl - 67781-252-01 - (theophylline anhydrous)
Drug Information of Uniphyl
| Product NDC: | 67781-252 |
| Proprietary Name: | Uniphyl |
| Non Proprietary Name: | theophylline anhydrous |
| Active Ingredient(s): | 600 mg/1 & nbsp; theophylline anhydrous |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Uniphyl
| Product NDC: | 67781-252 |
| Labeler Name: | Purdue Pharmaceutical Products LP |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040086 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960607 |
Package Information of Uniphyl
| Package NDC: | 67781-252-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (67781-252-01) |
NDC Information of Uniphyl
| NDC Code | 67781-252-01 |
| Proprietary Name | Uniphyl |
| Package Description | 100 TABLET in 1 BOTTLE (67781-252-01) |
| Product NDC | 67781-252 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | theophylline anhydrous |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19960607 |
| Marketing Category Name | ANDA |
| Labeler Name | Purdue Pharmaceutical Products LP |
| Substance Name | THEOPHYLLINE ANHYDROUS |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |
