Progesterone
NDC product · U.S. Food and Drug Administration (openFDA) · United States
-
Product NDC
76420-059 -
Package NDC
76420-059-10 -
Package NDC
76420-059-30 -
Package NDC
76420-059-90 -
Application number
ANDA207724 -
SPL ID
ead2bd7f-b5e3-3c69-e053-2995a90adf37 -
SPL set ID
19716042-8025-43a3-b26d-e0fd7d2587eb -
UNII
4G7DS2Q64Y -
RxCUI
260243 -
RxCUI
312641
What the source publishes
- Labeler
- Asclemed USA, Inc.
- Active ingredients
- Progesterone
- Form
- CAPSULE
- Routes
- ORAL
- Administrative status
- present-in-source-snapshot
- Marketing status
- ANDA
- Product type
- HUMAN PRESCRIPTION DRUG
- Prescription
- Prescription or restricted
Names this record is found by
Complete source data
{
"name": "Progesterone",
"splId": "ead2bd7f-b5e3-3c69-e053-2995a90adf37",
"labels": [
{
"setId": "19716042-8025-43a3-b26d-e0fd7d2587eb",
"labelUrl": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=19716042-8025-43a3-b26d-e0fd7d2587eb",
"labelPdfUrl": "https://dailymed.nlm.nih.gov/dailymed/downloadpdffile.cfm?setId=19716042-8025-43a3-b26d-e0fd7d2587eb"
}
],
"routes": [
"ORAL"
],
"labeler": "Asclemed USA, Inc.",
"finished": true,
"packaging": [
{
"sample": false,
"description": "100 CAPSULE in 1 BOTTLE (76420-059-10)",
"package_ndc": "76420-059-10",
"identifierStatus": "well-formed",
"marketing_start_date": "20191216"
},
{
"sample": false,
"description": "30 CAPSULE in 1 BOTTLE (76420-059-30)",
"package_ndc": "76420-059-30",
"identifierStatus": "well-formed",
"marketing_start_date": "20191216"
},
{
"sample": false,
"description": "90 CAPSULE in 1 BOTTLE (76420-059-90)",
"package_ndc": "76420-059-90",
"identifierStatus": "well-formed",
"marketing_start_date": "20191216"
}
],
"productId": "76420-059_ead2bd7f-b5e3-3c69-e053-2995a90adf37",
"useDomain": "unknown",
"dosageForm": "CAPSULE",
"productNdc": "76420-059",
"deaSchedule": null,
"genericName": "Progesterone",
"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": "PROGESTERONE",
"strength": "200 mg/1"
}
],
"applicationNumber": "ANDA207724",
"marketingCategory": "ANDA",
"stateRestrictions": {
"status": "not-collected",
"observations": []
},
"useDomainEvidence": {
"basis": "unreviewed",
"field": null,
"value": null,
"version": 1,
"sourceId": "us.fda.ndc"
},
"marketingStartDate": "20170911",
"targetSpeciesStatus": "not-reported",
"prescriptionCategory": "prescription-or-restricted",
"harmonizedIdentifiers": {
"nui": [
"M0017672",
"N0000175601"
],
"unii": [
"4G7DS2Q64Y"
],
"rxcui": [
"260243",
"312641"
],
"spl_set_id": [
"19716042-8025-43a3-b26d-e0fd7d2587eb"
],
"pharm_class_cs": [
"Progesterone [CS]"
],
"pharm_class_epc": [
"Progesterone [EPC]"
],
"manufacturer_name": [
"Asclemed USA, Inc."
]
},
"listingExpirationDate": "20271231"
}
Read this record from your own software
The same record, with every field and its provenance, is one request away. An API key is free and works immediately.
curl -G "https://api.medifontis.com/v1/drugs/record" \
-H "Authorization: Bearer $MEDIFONTIS_API_KEY" \
--data-urlencode "country=us" \
--data-urlencode "sourceId=us.fda.ndc" \
--data-urlencode "id=us:fda:ndc:76420-059_ead2bd7f-b5e3-3c69-e053-2995a90adf37"