pravastatin sodium

Generic: pravastatin sodium

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pravastatin sodium
Generic Name pravastatin sodium
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pravastatin sodium 20 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-5892
Product ID 0904-5892_1fc88a70-8c13-4db5-97e5-e0f356ce65aa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076341
Listing Expiration 2027-12-31
Marketing Start 2011-07-18

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 09045892
Hyphenated Format 0904-5892

Supplemental Identifiers

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 ANDA076341 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-5892-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-5892-61 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-5892-61) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

pravastatin sodium (20 mg/1)

Linked Drug Pages (1)

PRAVASTATIN SODIUM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1fc88a70-8c13-4db5-97e5-e0f356ce65aa", "openfda": {"unii": ["3M8608UQ61"], "spl_set_id": ["1d5bce9c-a788-4c52-a69e-c53174b8d061"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-5892-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-5892-61", "marketing_start_date": "20110718"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "0904-5892_1fc88a70-8c13-4db5-97e5-e0f356ce65aa", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "0904-5892", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20271231"}