Amerithroid
NDC product · U.S. Food and Drug Administration (openFDA) · United States
-
Product NDC
82685-341 -
Package NDC
82685-341-01 -
SPL ID
15d44dfd-e076-49df-89ef-ff40772e4b3e -
SPL set ID
03e79049-65b2-4f47-9c98-7ebb324cbc14 -
UNII
6RV024OAUQ -
RxCUI
198278 -
RxCUI
208545 -
RxCUI
313385 -
RxCUI
313387 -
RxCUI
313391 -
RxCUI
313393 -
RxCUI
314267 -
RxCUI
315235 -
RxCUI
2743051 -
RxCUI
2743053 -
RxCUI
2743055 -
RxCUI
2743057 -
RxCUI
2743059 -
RxCUI
2743061 -
RxCUI
2743063 -
RxCUI
2743065
What the source publishes
- Labeler
- Oliva Therapeutics, LLC
- Active ingredients
- THYROID
- Form
- TABLET
- Routes
- ORAL
- Administrative status
- present-in-source-snapshot
- Marketing status
- UNAPPROVED DRUG OTHER
- Product type
- HUMAN PRESCRIPTION DRUG
- Prescription
- Prescription or restricted
Names this record is found by
Complete source data
{
"name": "Amerithroid",
"splId": "15d44dfd-e076-49df-89ef-ff40772e4b3e",
"labels": [
{
"setId": "03e79049-65b2-4f47-9c98-7ebb324cbc14",
"labelUrl": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=03e79049-65b2-4f47-9c98-7ebb324cbc14",
"labelPdfUrl": "https://dailymed.nlm.nih.gov/dailymed/downloadpdffile.cfm?setId=03e79049-65b2-4f47-9c98-7ebb324cbc14"
}
],
"routes": [
"ORAL"
],
"labeler": "Oliva Therapeutics, LLC",
"finished": true,
"packaging": [
{
"sample": false,
"description": "100 TABLET in 1 BOTTLE (82685-341-01)",
"package_ndc": "82685-341-01",
"identifierStatus": "well-formed",
"marketing_start_date": "20260507"
}
],
"productId": "82685-341_15d44dfd-e076-49df-89ef-ff40772e4b3e",
"useDomain": "unknown",
"dosageForm": "TABLET",
"productNdc": "82685-341",
"deaSchedule": null,
"genericName": "THYROID",
"productType": "HUMAN PRESCRIPTION DRUG",
"listingStatus": "present-in-source-snapshot",
"targetSpecies": [],
"approvalStatus": "not-established-by-ndc-listing",
"labelAssociation": "openFDA-harmonized-set-ids; not a product-level approval match",
"marketingEndDate": null,
"activeIngredients": [
{
"name": "THYROID",
"strength": "15 mg/1"
}
],
"applicationNumber": null,
"marketingCategory": "UNAPPROVED DRUG OTHER",
"stateRestrictions": {
"status": "not-collected",
"observations": []
},
"useDomainEvidence": {
"basis": "unreviewed",
"field": null,
"value": null,
"version": 1,
"sourceId": "us.fda.ndc"
},
"marketingStartDate": "20260507",
"targetSpeciesStatus": "not-reported",
"prescriptionCategory": "prescription-or-restricted",
"harmonizedIdentifiers": {
"upc": [
"0382685346018",
"0382685341013",
"0382685343017",
"0382685342010",
"0382685348012",
"0382685344014",
"0382685345011",
"0382685347015"
],
"unii": [
"6RV024OAUQ"
],
"rxcui": [
"198278",
"208545",
"313385",
"313387",
"313391",
"313393",
"314267",
"315235",
"2743051",
"2743053",
"2743055",
"2743057",
"2743059",
"2743061",
"2743063",
"2743065"
],
"spl_set_id": [
"03e79049-65b2-4f47-9c98-7ebb324cbc14"
],
"manufacturer_name": [
"Oliva Therapeutics, LLC"
],
"is_original_packager": [
true
]
},
"listingExpirationDate": "20271231"
}
Read this record from your own software
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--data-urlencode "id=us:fda:ndc:82685-341_15d44dfd-e076-49df-89ef-ff40772e4b3e"