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NDC 50991-0323-01 Foltrate 500; 1 ug/1; mg/1 Details
Foltrate 500; 1 ug/1; mg/1
Foltrate is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Poly Pharmaceuticals, Inc.. The primary component is CYANOCOBALAMIN; FOLIC ACID.
Product Information
| NDC | 50991-0323 |
|---|---|
| Product ID | 50991-323_8751cbd7-0800-6f90-e053-2995a90acbd0 |
| Associated GPIs | 82991000000300 |
| GCN Sequence Number | 054713 |
| GCN Sequence Number Description | cyanocobalamin/folic acid TABLET 0.5 MG-1MG ORAL |
| HIC3 | C6L |
| HIC3 Description | VITAMIN B12 PREPARATIONS |
| GCN | 22758 |
| HICL Sequence Number | 001049 |
| HICL Sequence Number Description | CYANOCOBALAMIN/FOLIC ACID |
| Brand/Generic | Brand |
| Proprietary Name | Foltrate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Folic Acid and Cyanocobalamin |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 500; 1 |
| Active Ingredient Units | ug/1; mg/1 |
| Substance Name | CYANOCOBALAMIN; FOLIC ACID |
| Labeler Name | Poly Pharmaceuticals, Inc. |
| Pharmaceutical Class | Vitamin B 12 [CS], Vitamin B12 [EPC] |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | 2023-12-31 |
Package
NDC 50991-0323-01 (50991032301)
| NDC Package Code | 50991-323-01 |
|---|---|
| Billing NDC | 50991032301 |
| Package | 100 TABLET, FILM COATED in 1 BOTTLE (50991-323-01) |
| Marketing Start Date | 2010-08-26 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |