Lisinopril

Product NDC
63629-2935
11-digit product format
636292935
Labeler code
63629
Product ID
63629-2935_c9b876ae-2b64-45c8-97d8-7a3f0cd2ac46
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA076063
Marketing category
ANDA
Marketing start
2002-07-01
Marketing end
0000-00-00
Substance
LISINOPRIL
Active strength
40 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-2935-1EA - Each63629-2935e3fb8cfc-82ba-474f-8c88-e8a6eeb6eb0c12012-07-24
63629-2935-2EA - Each63629-2935627a1bd9-43ce-4e0c-8a42-c83351163faf12012-07-24
63629-2935-3EA - Each63629-293519ede913-fa37-49f0-bf2a-37835cd4d00412012-07-24
63629-2935-4EA - Each63629-29354fdda27f-a1a4-4d9c-9e2a-3cc45555260512012-07-24