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Lufyllin
Lufyllin - 0037-0731-92 - (Dyphylline)
Drug Information of Lufyllin
| Product NDC: | 0037-0731 |
| Proprietary Name: | Lufyllin |
| Non Proprietary Name: | Dyphylline |
| Active Ingredient(s): | 400 mg/1 & nbsp; Dyphylline |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lufyllin
| Product NDC: | 0037-0731 |
| Labeler Name: | Meda Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA084566 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19760831 |
Package Information of Lufyllin
| Package NDC: | 0037-0731-92 |
| Package Description: | 100 TABLET in 1 BOTTLE (0037-0731-92) |
NDC Information of Lufyllin
| NDC Code | 0037-0731-92 |
| Proprietary Name | Lufyllin |
| Package Description | 100 TABLET in 1 BOTTLE (0037-0731-92) |
| Product NDC | 0037-0731 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dyphylline |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19760831 |
| Marketing Category Name | NDA |
| Labeler Name | Meda Pharmaceuticals Inc. |
| Substance Name | DYPHYLLINE |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
