🇺🇸
United States · US · US:75907-237_46176916-f5b6-7f16-2601-3885bca7659f
Acid Reducer Powder
Orange BookUNIISPLATC A02BC
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDr. Reddy's Laboratories Inc.,
CountryUS (United States)
ATC codeA02BC
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11759072371414 PACKET in 1 CARTON (75907-237-14) / 1 POWDER, FOR SUSPENSION in 1 PACKET
- ndc11759072374242 PACKET in 1 CARTON (75907-237-42) / 1 POWDER, FOR SUSPENSION in 1 PACKET
Annotations
UNII (FDA Substance ID)
KG60484QX9
OMEPRAZOLE
RxCUI 7646
Orange Book
A217784
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "KG60484QX9",
"rxcui": "7646",
"inchikey": "SUBDBMMJDZJVOS-UHFFFAOYSA-N",
"display_name": "OMEPRAZOLE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"9826dd26-5592-4f96-9274-005ef9462cb4": {
"match": "brand_token",
"title": "ACID RELIEF (FAMOTIDINE) TABLET, FILM COATED [RITE AID CORPORATION]",
"spl_version": "5",
"published_date": "2026-05-28"
}
},
"productid": "75907-237_46176916-f5b6-7f16-2601-3885bca7659f",
"productndc": "75907-237",
"dosage_form": "POWDER, FOR SUSPENSION",
"orange_book": {
"appl_no": "217784",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "20MG/PACKET;1.68GM/PACKET",
"product_no": "001",
"approval_date": "May 9, 2024"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OMEPRAZOLE; SODIUM BICARBONATE",
"proprietary_name": "Acid Reducer Powder",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "ANDA217784",
"marketing_category": "ANDA",
"nonproprietary_name": "Omeprazole and Sodium Bicarbonate",
"start_marketing_date": "20240715",
"active_numerator_strength": "20; 1680"
}Related drugs
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