Nephron FA is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Nephro-tech, Inc.. The primary component is Iron; Ascorbic Acid; Niacinamide; Pyridoxine Hydrochloride; Pantothenic Acid; Riboflavin; Thiamine; Folic Acid; Biotin; Cobalamin.
| Product ID | 59528-4456_43a37439-b71f-4894-b7a1-f8d0af2c1212 |
| NDC | 59528-4456 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Nephron FA |
| Generic Name | Mineral/vitamin Supplement |
| Dosage Form | Tablet, Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 1992-11-01 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Nephro-Tech, Inc. |
| Substance Name | IRON; ASCORBIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; PANTOTHENIC ACID; RIBOFLAVIN; THIAMINE; FOLIC ACID; BIOTIN; COBALAMIN |
| Active Ingredient Strength | 66 mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1 |
| Pharm Classes | Vitamin C [EPC],Ascorbic Acid [CS],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 1992-11-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1992-11-01 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| IRON | 66 mg/1 |
| SPL SET ID: | a709f56a-08d0-4fe5-a9ed-e237a745be97 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 59528-4456 | Nephron FA | mineral/vitamin supplement |
| 68151-3063 | Nephron FA | mineral/vitamin supplement |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NEPHRON FA 74311197 1852852 Live/Registered |
NEPHRO-TECH, INC. 1992-09-04 |