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Fiber Lax
Fiber Lax - 0615-5532-31 - (CALCIUM POLYCARBOPHIL)
Drug Information of Fiber Lax
| Product NDC: | 0615-5532 |
| Proprietary Name: | Fiber Lax |
| Non Proprietary Name: | CALCIUM POLYCARBOPHIL |
| Active Ingredient(s): | 625 mg/1 & nbsp; CALCIUM POLYCARBOPHIL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fiber Lax
| Product NDC: | 0615-5532 |
| Labeler Name: | NCS HealthCare of KY, Inc dba Vangard Labs |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part334 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100901 |
Package Information of Fiber Lax
| Package NDC: | 0615-5532-31 |
| Package Description: | 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-5532-31) |
NDC Information of Fiber Lax
| NDC Code | 0615-5532-31 |
| Proprietary Name | Fiber Lax |
| Package Description | 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-5532-31) |
| Product NDC | 0615-5532 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CALCIUM POLYCARBOPHIL |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NCS HealthCare of KY, Inc dba Vangard Labs |
| Substance Name | CALCIUM POLYCARBOPHIL |
| Strength Number | 625 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
