Pravastatin sodium

Product NDC
68788-7193
11-digit product format
687887193
Labeler code
68788
Product ID
68788-7193_77d581ee-7d09-4408-ab06-336c3a8e482e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pravastatin sodium
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA076714
Marketing category
ANDA
Marketing start
2018-07-18
Marketing end
0000-00-00
Substance
PRAVASTATIN SODIUM
Active strength
80 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7193-1EA - Each68788-7193ce3d76a1-e07c-436b-b181-312a763ccb5912018-09-05
68788-7193-2EA - Each68788-7193c741fcdb-99d8-4ac3-b00a-db8af84fd3ef12018-09-05
68788-7193-3EA - Each68788-7193a10e1c12-6ae1-42af-aaca-014e1349777812018-09-05
68788-7193-6EA - Each68788-71937ff88584-8349-487b-a1c2-d9e2e2722e3912018-09-05
68788-7193-8EA - Each68788-7193f54b1c48-8e40-475e-9fec-05ec214913c512018-09-05
68788-7193-9EA - Each68788-7193dcdc5649-795e-4fd1-93a7-6b62c9b0458112018-09-05