NDC 0143-1248 - Folic Acid
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 0143-1248
- Package NDCs from labels
- 0143-1248-09, 0143-1248-01, 0143-1248-10, 0143-1248-25
- Manufacturer
- McKesson Packaging Services Business Unit of McKesson Corporation. | McKesson Packaging Services Business Unit of McKesson Corporation
- Effective date
- 2015-06-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FOLIC ACID TABLETS, USP | McKesson Packaging Services Business Unit of McKesson Corporation. | McKesson Packaging Services Business Unit of McKesson Corporation | 2015-06-09 | HUMAN PRESCRIPTION DRUG LABEL |
| Folic Acid - State of Florida DOH Central Pharmacy | State of Florida DOH Central Pharmacy | 2010-06-02 | HUMAN PRESCRIPTION DRUG LABEL |
| Folic Acid - Contract Pharmacy Services-PA | Contract Pharmacy Services-PA | 2010-04-12 | HUMAN PRESCRIPTION DRUG LABEL |
| FOLIC ACID TABLETS, USP | West-ward Pharmaceutical Corp. | 2007-05-28 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0143-1248-01 | Folic Acid | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | 1 | |
| 0143-1248-09 | Folic Acid | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | 1 | |
| 0143-1248-10 | Folic Acid | 1000 in 1 BOTTLE, PLASTIC | TABLET | 1000 | 1 | |
| 0143-1248-25 | Folic Acid | 100 in 1 BOX, UNIT-DOSE | TABLET | 100 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0143-1248-01 | EA - Each | 0143-1248 | f26243be-0b37-4859-8961-c9351e63ca2c | 1 | 2013-02-13 |
| 0143-1248-10 | EA - Each | 0143-1248 | 95dc56ff-ad71-4de4-8c2a-32bb68d0e142 | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Tox-Chord | ALFALFA, ALUMINA, BENZOICUM ACIDUM, CARBONEUM, CETRARIA ISLANDICA, FOLLICULINUM, FUCUS VESICULOSUS, FUMARICUM ACIDUM, HEPAR SUIS, KALI CARBONICUM, KREOSOTUM, NATRUM MURIATICUM, PARAFFINUM, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, PIX LIQUIDA, PLANTAGO MAJOR, PLUMBUM METALLICUM, PULSATILLA (VULGARIS), RADIUM BROMATUM, RESORCINUM, SALOL, SILICEA, SYMPHYTUM OFFICINALE, TABACUM, TEREBINTHINA, THYROIDINUM (BOVINE), TRITICUM REPENS, ZINCUM OXYDATUM | Energetix Corp | 6b0d1628-b20d-426e-9c84-5cceadca3f45 | 2016-11-11 | Warnings | ETJ7Z6XBU4 |
| Thyrotox | CHONDRUS CRISPUS, FUCUS VESICULOSUS, THYROIDINUM, BELLADONNA, CALCAREA CARBONICA, CONIUM MACULATUM, IODIUM, KALI CARBONICUM, PHOSPHORUS, PULSATILLA (VULGARIS), SILICEA | BioActive Nutritional, Inc. | e229a260-13f3-4136-b325-9a8954f8a327 | 2016-08-10 | Warnings | ETJ7Z6XBU4 |
| Teething | ARNICA MONTANA, TRIFOLIUM PRATENSE, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CHAMOMILLA, KREOSOTUM, SILICEA | BioActive Nutritional, Inc. | f39c9feb-f567-43a2-a026-2a581aeeed9d | 2016-07-27 | Warnings | ETJ7Z6XBU4 |
| 3d205ce1-db62-4a8b-931b-ec5d43dceacb | 61d4f671-10a2-4aff-8012-e9d4fecf15cc | 2010-06-02 | Warnings, Adverse reactions | 3d205ce1-db62-4a8b-931b-ec5d43dceacb 61d4f671-10a2-4aff-8012-e9d4fecf15cc | ||
| b561a04c-b0a6-4da1-9955-172672f10669 | b561a04c-b0a6-4da1-9955-172672f10669 | 2010-04-12 | Warnings, Adverse reactions | b561a04c-b0a6-4da1-9955-172672f10669 b561a04c-b0a6-4da1-9955-172672f10669 | ||
| 0CD0BD38-EB3D-A57E-7F08-309F45C517F5 | 748977db-fd10-46b8-a219-381ba34e55cd | 2007-05-28 | Warnings, Adverse reactions | 0CD0BD38-EB3D-A57E-7F08-309F45C517F5 748977db-fd10-46b8-a219-381ba34e55cd |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.