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United States · US · US:43598-294_4a1e5038-d049-606f-c087-48bc353a8a69
pregabalin
Orange BookUNIISPLATC N02BF02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDr.Reddys Laboratories Inc
CountryUS (United States)
ATC codeN02BF02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc114359829405500 CAPSULE in 1 BOTTLE (43598-294-05)
- ndc1143598294665 BLISTER PACK in 1 CARTON (43598-294-66) / 10 CAPSULE in 1 BLISTER PACK (43598-294-79)
- ndc11435982947810 BLISTER PACK in 1 CARTON (43598-294-78) / 10 CAPSULE in 1 BLISTER PACK (43598-294-79)
- ndc11435982949090 CAPSULE in 1 BOTTLE (43598-294-90)
Annotations
UNII (FDA Substance ID)
55JG375S6M
PREGABALIN
RxCUI 187832
Orange Book
A209664
ABABABABABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "55JG375S6M",
"rxcui": "187832",
"inchikey": "AYXYPKUFHZROOJ-ZETCQYMHSA-N",
"display_name": "PREGABALIN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"34846423-e747-42c5-9bcd-f99c557c4f67": {
"match": "brand_token",
"title": "PREGABALIN CAPSULE [PROFICIENT RX LP]",
"spl_version": "1",
"published_date": "2026-05-29"
}
},
"productid": "43598-294_4a1e5038-d049-606f-c087-48bc353a8a69",
"productndc": "43598-294",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "209664",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "001",
"approval_date": "Jul 19, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG",
"product_no": "002",
"approval_date": "Jul 19, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "75MG",
"product_no": "003",
"approval_date": "Jul 19, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "100MG",
"product_no": "004",
"approval_date": "Jul 19, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "150MG",
"product_no": "005",
"approval_date": "Jul 19, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "200MG",
"product_no": "006",
"approval_date": "Jul 19, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "225MG",
"product_no": "007",
"approval_date": "Jul 19, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "300MG",
"product_no": "008",
"approval_date": "Jul 19, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": "CV",
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PREGABALIN",
"proprietary_name": "pregabalin",
"active_ingred_unit": "mg/1",
"application_number": "ANDA209664",
"marketing_category": "ANDA",
"nonproprietary_name": "pregabalin",
"start_marketing_date": "20190719",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code N02BF02.
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