adverse reactions
ADVERSE REACTIONS: Allergic sensitization has been reported following both oral and parenteral administration of folic acid.
Prenate Chewable
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Prenate Chewable
- Generic name
- CALCIUM CARBONATE, CHOLECALCIFEROL, MAGNESIUM OXIDE, BORON, FOLIC ACID, LEVOMEFOLATE GLUCOSAMINE, PYRIDOXINE HYDROCHLORIDE, CYANOCOBALAMIN, BIOTIN AND BLUEBERRY
- Manufacturer
- Avion Pharmaceuticals, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 917f02ce-51b9-4819-81e0-522842f6732a
- SPL ID
- 446d4734-3924-b589-e063-6394a90ab23f
- Version
- 10
- Effective date
- 2025-11-25
- Source export date
- 2026-10-12
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:44:58
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Prenate Chewable | openfda.brand_name | |
| generic name | CALCIUM CARBONATE, CHOLECALCIFEROL, MAGNESIUM OXIDE, BORON, FOLIC ACID, LEVOMEFOLATE GLUCOSAMINE, PYRIDOXINE HYDROCHLORIDE, CYANOCOBALAMIN, BIOTIN AND BLUEBERRY | openfda.generic_name | |
| manufacturer name | Avion Pharmaceuticals, LLC | openfda.manufacturer_name | |
| ndc | package | 75854-306-30 | openfda.package_ndc |
| ndc | product | 75854-306 | openfda.product_ndc |
| ndc11 | package | 75854030630 | derived:openfda.package_ndc |
| spl id | 446d4734-3924-b589-e063-6394a90ab23f | id | |
| spl set id | 917f02ce-51b9-4819-81e0-522842f6732a | set_id | |
| unii | N9E3X5056Q | openfda.unii | |
| unii | H0G9379FGK | openfda.unii | |
| unii | 935E97BOY8 | openfda.unii | |
| unii | Q65PL71Q1A | openfda.unii | |
| unii | 3A3U0GI71G | openfda.unii | |
| unii | 6SO6U10H04 | openfda.unii | |
| unii | P6YC3EG204 | openfda.unii | |
| unii | 253RUG1X1A | openfda.unii | |
| unii | 68Y4CF58BV | openfda.unii | |
| unii | 1C6V77QF41 | openfda.unii |
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.