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United States · US · US:90096-161_1e574b03-a038-453b-b84f-9437fc2df0f8
Naproxen
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerZameer Pharmaceuticals LLC
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc119009616101100 TABLET, DELAYED RELEASE in 1 BOTTLE (90096-161-01)
Annotations
UNII (FDA Substance ID)
57Y76R9ATQ
NAPROXEN
RxCUI 7258
Orange Book
N020067
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "57Y76R9ATQ",
"rxcui": "7258",
"inchikey": "CMWTZPSULFXXJA-VIFPVBQESA-N",
"display_name": "NAPROXEN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c5146d73-2f34-4dfe-ac29-97071279dc4d": {
"match": "brand_token",
"title": "NAPROXEN SODIUM TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]",
"spl_version": "10",
"published_date": "2026-05-28"
}
},
"productid": "90096-161_1e574b03-a038-453b-b84f-9437fc2df0f8",
"productndc": "90096-161",
"dosage_form": "TABLET, DELAYED RELEASE",
"orange_book": {
"appl_no": "020067",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "375MG",
"product_no": "002",
"approval_date": "Oct 14, 1994"
},
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "500MG",
"product_no": "003",
"approval_date": "Oct 14, 1994"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NAPROXEN",
"proprietary_name": "Naproxen",
"active_ingred_unit": "mg/1",
"application_number": "NDA020067",
"marketing_category": "NDA AUTHORIZED GENERIC",
"nonproprietary_name": "Naproxen",
"start_marketing_date": "20250831",
"active_numerator_strength": "500"
}Related drugs
Other records sharing ATC code G02CC02.
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