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ELIXOPHYLLIN
ELIXOPHYLLIN - 49708-644-90 - (THEOPHYLLINE ANHYDROUS)
Drug Information of ELIXOPHYLLIN
| Product NDC: | 49708-644 |
| Proprietary Name: | ELIXOPHYLLIN |
| Non Proprietary Name: | THEOPHYLLINE ANHYDROUS |
| Active Ingredient(s): | 80 mg/15mL & nbsp; THEOPHYLLINE ANHYDROUS |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ELIXOPHYLLIN
| Product NDC: | 49708-644 |
| Labeler Name: | Caraco Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA085186 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091001 |
Package Information of ELIXOPHYLLIN
| Package NDC: | 49708-644-90 |
| Package Description: | 473 mL in 1 BOTTLE (49708-644-90) |
NDC Information of ELIXOPHYLLIN
| NDC Code | 49708-644-90 |
| Proprietary Name | ELIXOPHYLLIN |
| Package Description | 473 mL in 1 BOTTLE (49708-644-90) |
| Product NDC | 49708-644 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | THEOPHYLLINE ANHYDROUS |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20091001 |
| Marketing Category Name | ANDA |
| Labeler Name | Caraco Pharma, Inc. |
| Substance Name | THEOPHYLLINE ANHYDROUS |
| Strength Number | 80 |
| Strength Unit | mg/15mL |
| Pharmaceutical Classes | Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |
