pregabalin
Generic: pregabalin
Labeler: westminster pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
pregabalin
Generic Name
pregabalin
Labeler
westminster pharmaceuticals, llc
Dosage Form
CAPSULE
Routes
Active Ingredients
pregabalin 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69367-324
Product ID
69367-324_0efc2eea-ebae-47f9-a13a-f2df4331cf04
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208677
DEA Schedule
cv
Listing Expiration
2026-12-31
Marketing Start
2021-08-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69367324
Hyphenated Format
69367-324
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
pregabalin (source: ndc)
Generic Name
pregabalin (source: ndc)
Application Number
ANDA208677 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 90 CAPSULE in 1 BOTTLE (69367-324-09)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0efc2eea-ebae-47f9-a13a-f2df4331cf04", "openfda": {"upc": ["0369367328098", "0369367330091", "0369367327091", "0369367326094", "0369367325097", "0369367324090", "0369367331098", "0369367329095"], "unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450", "577127"], "spl_set_id": ["781cb1ac-a0d2-4b47-b319-f0b90de86384"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (69367-324-09)", "package_ndc": "69367-324-09", "marketing_start_date": "20210824"}], "brand_name": "Pregabalin", "product_id": "69367-324_0efc2eea-ebae-47f9-a13a-f2df4331cf04", "dosage_form": "CAPSULE", "product_ndc": "69367-324", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "25 mg/1"}], "application_number": "ANDA208677", "marketing_category": "ANDA", "marketing_start_date": "20210824", "listing_expiration_date": "20261231"}