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 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6503
Product ID 50090-6503_42e540fd-d842-4ec4-b20b-66c9038c3198
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209357
DEA Schedule cv
Listing Expiration 2027-12-31
Marketing Start 2019-07-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906503
Hyphenated Format 50090-6503

Supplemental Identifiers

RxCUI
483438
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 ANDA209357 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 60 CAPSULE in 1 BOTTLE (50090-6503-0)
source: ndc

Packages (1)

Ingredients (1)

pregabalin (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42e540fd-d842-4ec4-b20b-66c9038c3198", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483438"], "spl_set_id": ["217c9f93-fe89-4684-8553-12ec9acaa507"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (50090-6503-0)", "package_ndc": "50090-6503-0", "marketing_start_date": "20230526"}], "brand_name": "Pregabalin", "product_id": "50090-6503_42e540fd-d842-4ec4-b20b-66c9038c3198", "dosage_form": "CAPSULE", "product_ndc": "50090-6503", "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": "100 mg/1"}], "application_number": "ANDA209357", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20271231"}