pregabalin

Generic: pregabalin

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler a-s medication solutions
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

pregabalin 75 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6793
Product ID 50090-6793_33934149-bafc-4450-978f-b141f6d0deed
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210432
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2019-07-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906793
Hyphenated Format 50090-6793

Supplemental Identifiers

RxCUI
483450
UNII
55JG375S6M

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 ANDA210432 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE (50090-6793-0)
  • 60 CAPSULE in 1 BOTTLE (50090-6793-1)
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": "33934149-bafc-4450-978f-b141f6d0deed", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483450"], "spl_set_id": ["54a9bfb4-dcff-491d-9676-1fe1d05e004c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-6793-0)", "package_ndc": "50090-6793-0", "marketing_start_date": "20231101"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (50090-6793-1)", "package_ndc": "50090-6793-1", "marketing_start_date": "20250509"}], "brand_name": "PREGABALIN", "product_id": "50090-6793_33934149-bafc-4450-978f-b141f6d0deed", "dosage_form": "CAPSULE", "product_ndc": "50090-6793", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREGABALIN", "active_ingredients": [{"name": "PREGABALIN", "strength": "75 mg/1"}], "application_number": "ANDA210432", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}