🇺🇸
United States · US · US:69953-516_f0fabe80-87bc-9b65-e053-2995a90a582b
Morning After
Orange BookUNIISPLATC G03AD01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRapha Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeG03AD01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1169953516011 BLISTER PACK in 1 CARTON (69953-516-01) / 1 mg in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
5W7SIA7YZW
LEVONORGESTREL
RxCUI 6373
Orange Book
A205329
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "5W7SIA7YZW",
"rxcui": "6373",
"inchikey": "WWYNJERNGUHSAO-XUDSTZEESA-N",
"display_name": "LEVONORGESTREL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"2a42d8ce-e7f2-caa5-e063-6294a90ac01f": {
"match": "brand_token",
"title": "MORNING FRESH MINT TOOTHPASTE, WITH FLUORIDE PASTE [DYNAREX CORPORATION]",
"spl_version": "3",
"published_date": "2026-05-11"
}
},
"productid": "69953-516_f0fabe80-87bc-9b65-e053-2995a90a582b",
"productndc": "69953-516",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "205329",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "1.5MG",
"product_no": "001",
"approval_date": "Sep 18, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LEVONORGESTREL",
"proprietary_name": "Morning After",
"active_ingred_unit": "mg/1.5mg",
"application_number": "ANDA205329",
"marketing_category": "ANDA",
"nonproprietary_name": "Levonorgestrel",
"start_marketing_date": "20221230",
"active_numerator_strength": "1.5"
}Related drugs
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