| Product NDC: | 50474-300 |
| Proprietary Name: | Theo-24 |
| Non Proprietary Name: | theophylline anhydrous |
| Active Ingredient(s): | 300 mg/1 & nbsp; theophylline anhydrous |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50474-300 |
| Labeler Name: | UCB, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087944 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19980220 |
| Package NDC: | 50474-300-50 |
| Package Description: | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50474-300-50) |
| NDC Code | 50474-300-50 |
| Proprietary Name | Theo-24 |
| Package Description | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50474-300-50) |
| Product NDC | 50474-300 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | theophylline anhydrous |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19980220 |
| Marketing Category Name | ANDA |
| Labeler Name | UCB, Inc. |
| Substance Name | THEOPHYLLINE ANHYDROUS |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |