pregabalin

Generic: pregabalin

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler westminster pharmaceuticals, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

pregabalin 75 mg/1

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-426
Product ID 69367-426_da37b9bc-466b-4bef-8c28-36586538df59
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212988
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2025-11-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367426
Hyphenated Format 69367-426

Supplemental Identifiers

RxCUI
483438 483440 483442 483444 483446 483448 483450 577127
UPC
0369367428095 0369367427098 0369367426091 0369367425094 0369367424097 0369367431095 0369367429092
UNII
55JG375S6M

Packaging Origin

Original Packager
true

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 ANDA212988 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 500 CAPSULE in 1 BOTTLE (69367-426-05)
  • 90 CAPSULE in 1 BOTTLE (69367-426-09)
source: ndc

Packages (2)

Ingredients (1)

pregabalin (75 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "da37b9bc-466b-4bef-8c28-36586538df59", "openfda": {"upc": ["0369367428095", "0369367427098", "0369367426091", "0369367425094", "0369367424097", "0369367431095", "0369367429092"], "unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450", "577127"], "spl_set_id": ["6b0ee2cf-52c3-4052-bea0-1458a4233745"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (69367-426-05)", "package_ndc": "69367-426-05", "marketing_start_date": "20251117"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (69367-426-09)", "package_ndc": "69367-426-09", "marketing_start_date": "20251117"}], "brand_name": "Pregabalin", "product_id": "69367-426_da37b9bc-466b-4bef-8c28-36586538df59", "dosage_form": "CAPSULE", "product_ndc": "69367-426", "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": "75 mg/1"}], "application_number": "ANDA212988", "marketing_category": "ANDA", "marketing_start_date": "20251117", "listing_expiration_date": "20261231"}