pregabalin

Generic: pregabalin

Labeler: mylan pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler mylan pharmaceuticals inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

pregabalin 20 mg/mL

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 59762-1576
Product ID 59762-1576_7aa334e7-3c46-4680-a266-9049af3bf566
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA022488
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2019-07-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 597621576
Hyphenated Format 59762-1576

Supplemental Identifiers

RxCUI
898715
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 NDA022488 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (59762-1576-1) / 473 mL in 1 BOTTLE
source: ndc

Packages (1)

59762-1576-1 1 BOTTLE in 1 CARTON (59762-1576-1) / 473 mL in 1 BOTTLE

Ingredients (1)

pregabalin (20 mg/mL)

Linked Drug Pages (1)

Pregabalin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7aa334e7-3c46-4680-a266-9049af3bf566", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["898715"], "spl_set_id": ["ebe34db4-816d-4f0a-adbb-826693662754"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59762-1576-1)  / 473 mL in 1 BOTTLE", "package_ndc": "59762-1576-1", "marketing_start_date": "20190729"}], "brand_name": "Pregabalin", "product_id": "59762-1576_7aa334e7-3c46-4680-a266-9049af3bf566", "dosage_form": "SOLUTION", "product_ndc": "59762-1576", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "20 mg/mL"}], "application_number": "NDA022488", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190729", "listing_expiration_date": "20261231"}