pravastatin sodium

Generic: pravastatin sodium

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pravastatin sodium
Generic Name pravastatin sodium
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pravastatin sodium 10 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-886
Product ID 60687-886_4600582d-4c2e-b8ce-e063-6394a90ace45
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077987
Listing Expiration 2026-12-31
Marketing Start 2025-03-02

Pharmacologic Class

Classes
hmg-coa reductase inhibitor [epc] hydroxymethylglutaryl-coa reductase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687886
Hyphenated Format 60687-886

Supplemental Identifiers

RxCUI
904458 904467 904475
UNII
3M8608UQ61

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 ANDA077987 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (60687-886-01) / 1 TABLET in 1 BLISTER PACK (60687-886-11)
source: ndc

Packages (1)

Ingredients (1)

pravastatin sodium (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4600582d-4c2e-b8ce-e063-6394a90ace45", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475"], "spl_set_id": ["97f826f0-b5c5-410c-b1f0-523873981e8d"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-886-01)  / 1 TABLET in 1 BLISTER PACK (60687-886-11)", "package_ndc": "60687-886-01", "marketing_start_date": "20250302"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "60687-886_4600582d-4c2e-b8ce-e063-6394a90ace45", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "60687-886", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA077987", "marketing_category": "ANDA", "marketing_start_date": "20250302", "listing_expiration_date": "20261231"}