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 50090-5038
Product ID 50090-5038_ec6d3b8b-92b8-4def-98cb-ee905069cb64
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208677
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 500905038
Hyphenated Format 50090-5038

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 ANDA208677 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE (50090-5038-0)
  • 60 CAPSULE in 1 BOTTLE (50090-5038-1)
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": "ec6d3b8b-92b8-4def-98cb-ee905069cb64", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483450"], "spl_set_id": ["55b62778-0e6a-45e8-9ace-3f1d6eca4487"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-5038-0)", "package_ndc": "50090-5038-0", "marketing_start_date": "20200508"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (50090-5038-1)", "package_ndc": "50090-5038-1", "marketing_start_date": "20241022"}], "brand_name": "Pregabalin", "product_id": "50090-5038_ec6d3b8b-92b8-4def-98cb-ee905069cb64", "dosage_form": "CAPSULE", "product_ndc": "50090-5038", "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": "ANDA208677", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20271231"}