pregabalin

Generic: pregabalin

Labeler: sciegen pharmaceuticals, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler sciegen pharmaceuticals, inc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

pregabalin 225 mg/1

Manufacturer
ScieGen Pharmaceuticals, Inc

Identifiers & Regulatory

Product NDC 50228-356
Product ID 50228-356_955253a7-d80a-44ef-83c4-74b33ee6a622
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208677
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 50228356
Hyphenated Format 50228-356

Supplemental Identifiers

RxCUI
483438 483440 483442 483444 483446 483448 483450 577127
UPC
0350228356053 0350228354301 0350228355056 0350228357050 0350228352901 0350228357906 0350228356909 0350228350907 0350228354103 0350228350105 0350228353908 0350228351904 0350228354905 0350228355902 0350228352307 0350228352109 0350228353106 0350228351102
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 ANDA208677 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 225 mg/1
source: ndc
Packaging
  • 500 CAPSULE in 1 BOTTLE (50228-356-05)
  • 30 CAPSULE in 1 BOTTLE (50228-356-30)
  • 90 CAPSULE in 1 BOTTLE (50228-356-90)
source: ndc

Packages (3)

50228-356-05 500 CAPSULE in 1 BOTTLE (50228-356-05) 50228-356-30 30 CAPSULE in 1 BOTTLE (50228-356-30) 50228-356-90 90 CAPSULE in 1 BOTTLE (50228-356-90)

Ingredients (1)

pregabalin (225 mg/1)

Linked Drug Pages (1)

Pregabalin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "955253a7-d80a-44ef-83c4-74b33ee6a622", "openfda": {"upc": ["0350228356053", "0350228354301", "0350228355056", "0350228357050", "0350228352901", "0350228357906", "0350228356909", "0350228350907", "0350228354103", "0350228350105", "0350228353908", "0350228351904", "0350228354905", "0350228355902", "0350228352307", "0350228352109", "0350228353106", "0350228351102"], "unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450", "577127"], "spl_set_id": ["33ef1a3b-554f-4a51-afdb-92a019e8c16c"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (50228-356-05)", "package_ndc": "50228-356-05", "marketing_start_date": "20190719"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50228-356-30)", "package_ndc": "50228-356-30", "marketing_start_date": "20190719"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50228-356-90)", "package_ndc": "50228-356-90", "marketing_start_date": "20190719"}], "brand_name": "Pregabalin", "product_id": "50228-356_955253a7-d80a-44ef-83c4-74b33ee6a622", "dosage_form": "CAPSULE", "product_ndc": "50228-356", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "ScieGen Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "225 mg/1"}], "application_number": "ANDA208677", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}