pregabalin

Generic: pregabalin

Labeler: patrin pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler patrin pharma, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

pregabalin 20 mg/mL

Manufacturer
Patrin Pharma, Inc.

Identifiers & Regulatory

Product NDC 39328-090
Product ID 39328-090_3a08157d-abaf-445c-b333-c209ef961bc0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212604
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2022-06-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 39328090
Hyphenated Format 39328-090

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 ANDA212604 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (39328-090-16) / 473 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

39328-090-16 1 BOTTLE, PLASTIC in 1 CARTON (39328-090-16) / 473 mL in 1 BOTTLE, PLASTIC

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": "3a08157d-abaf-445c-b333-c209ef961bc0", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["898715"], "spl_set_id": ["d92c94e5-e542-4177-afa8-fa00ba17634c"], "manufacturer_name": ["Patrin Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (39328-090-16)  / 473 mL in 1 BOTTLE, PLASTIC", "package_ndc": "39328-090-16", "marketing_start_date": "20220614"}], "brand_name": "PREGABALIN", "product_id": "39328-090_3a08157d-abaf-445c-b333-c209ef961bc0", "dosage_form": "SOLUTION", "product_ndc": "39328-090", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Patrin Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREGABALIN", "active_ingredients": [{"name": "PREGABALIN", "strength": "20 mg/mL"}], "application_number": "ANDA212604", "marketing_category": "ANDA", "marketing_start_date": "20220614", "listing_expiration_date": "20261231"}