pravastatin sodium
Generic: pravastatin sodium
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
pravastatin sodium
Generic Name
pravastatin sodium
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
pravastatin sodium 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51655-708
Product ID
51655-708_4951021b-e7bd-d11f-e063-6294a90aa15f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076341
Listing Expiration
2027-12-31
Marketing Start
2021-05-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51655708
Hyphenated Format
51655-708
Supplemental Identifiers
RxCUI
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
pravastatin sodium (source: ndc)
Generic Name
pravastatin sodium (source: ndc)
Application Number
ANDA076341 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (51655-708-52)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4951021b-e7bd-d11f-e063-6294a90aa15f", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["db5b8821-dca8-9322-e053-2a95a90abdc3"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-708-52)", "package_ndc": "51655-708-52", "marketing_start_date": "20210521"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "51655-708_4951021b-e7bd-d11f-e063-6294a90aa15f", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "51655-708", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20210521", "listing_expiration_date": "20271231"}