pregabalin
Generic: pregabalin
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
pregabalin
Generic Name
pregabalin
Labeler
proficient rx lp
Dosage Form
CAPSULE
Routes
Active Ingredients
pregabalin 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-556
Product ID
71205-556_f58c99d0-e792-46b7-a67c-c6b1bce50946
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
71205556
Hyphenated Format
71205-556
Supplemental Identifiers
RxCUI
UPC
UNII
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
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (71205-556-30)
- 60 CAPSULE in 1 BOTTLE (71205-556-60)
- 90 CAPSULE in 1 BOTTLE (71205-556-90)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f58c99d0-e792-46b7-a67c-c6b1bce50946", "openfda": {"upc": ["0371205556303"], "unii": ["55JG375S6M"], "rxcui": ["483448"], "spl_set_id": ["89b8c2d2-4a99-4b97-8b82-c0c36cd0df1b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71205-556-30)", "package_ndc": "71205-556-30", "marketing_start_date": "20210423"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71205-556-60)", "package_ndc": "71205-556-60", "marketing_start_date": "20210423"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71205-556-90)", "package_ndc": "71205-556-90", "marketing_start_date": "20210423"}], "brand_name": "Pregabalin", "product_id": "71205-556_f58c99d0-e792-46b7-a67c-c6b1bce50946", "dosage_form": "CAPSULE", "product_ndc": "71205-556", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "50 mg/1"}], "application_number": "ANDA208677", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}