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FIBERCON
FIBERCON - 0005-2500-33 - (CALCIUM POLYCARBOPHIL)
Drug Information of FIBERCON
| Product NDC: | 0005-2500 |
| Proprietary Name: | FIBERCON |
| Non Proprietary Name: | CALCIUM POLYCARBOPHIL |
| Active Ingredient(s): | 625 mg/1 & nbsp; CALCIUM POLYCARBOPHIL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FIBERCON
| Product NDC: | 0005-2500 |
| Labeler Name: | Wyeth Pharmaceutical Division of Wyeth Holdings Corporation, a subsidiary of Pfizer Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20040105 |
Package Information of FIBERCON
| Package NDC: | 0005-2500-33 |
| Package Description: | 1 BOTTLE in 1 CARTON (0005-2500-33) > 90 TABLET in 1 BOTTLE |
NDC Information of FIBERCON
| NDC Code | 0005-2500-33 |
| Proprietary Name | FIBERCON |
| Package Description | 1 BOTTLE in 1 CARTON (0005-2500-33) > 90 TABLET in 1 BOTTLE |
| Product NDC | 0005-2500 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CALCIUM POLYCARBOPHIL |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040105 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Wyeth Pharmaceutical Division of Wyeth Holdings Corporation, a subsidiary of Pfizer Inc. |
| Substance Name | CALCIUM POLYCARBOPHIL |
| Strength Number | 625 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
