🇺🇸
United States · US · US:63029-656_ada25630-e145-4866-b173-435441e2688a
GOODYS PM
In shortageUNIISPLATC N02BE
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMedtech Products Inc.
CountryUS (United States)
ATC codeN02BE
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1163029656066 POWDER in 1 CARTON (63029-656-06)
- ndc11630296561616 POWDER in 1 CARTON (63029-656-16)
Annotations
UNII (FDA Substance ID)
362O9ITL9D
ACETAMINOPHEN
RxCUI 161
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Acetaminophen; Oxycodone Hydrochloride Tablet
Raw payload (JSON)
{
"unii": {
"unii": "362O9ITL9D",
"rxcui": "161",
"inchikey": "RZVAJINKPMORJF-UHFFFAOYSA-N",
"display_name": "ACETAMINOPHEN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"02b3a604-3f09-47e7-add1-b9038b3a268b": {
"match": "brand_token",
"title": "GOODYS MAX (ACETAMINOPHEN, ASPIRIN, AND CAFFEINE) POWDER [MEDTECH PRODUCTS INC.]",
"spl_version": "1",
"published_date": "2026-02-02"
}
},
"productid": "63029-656_ada25630-e145-4866-b173-435441e2688a",
"productndc": "63029-656",
"dosage_form": "POWDER",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ACETAMINOPHEN; DIPHENHYDRAMINE CITRATE",
"shortage_reason": "Acetaminophen; Oxycodone Hydrochloride Tablet",
"shortage_status": "current",
"proprietary_name": "GOODYS PM",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "M013",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Acetaminophen and Diphenhydramine Citrate",
"start_marketing_date": "20130901",
"active_numerator_strength": "500; 38"
}Related drugs
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- 🇺🇸Acetaminophen 250 mg and Ibuprofen 125 mgR J General Corporation
- 🇺🇸Acetaminophen 250 mg and Ibuprofen 125 mgSun Pharmaceutical Industries, Inc.
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