Ramipril

Product NDC
68382-375
11-digit product format
683820375
Labeler code
68382
Product ID
68382-375_0fcc9d88-ecff-40db-a5bf-870d917146ea
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ramipril
Dosage form
TABLET
Route
ORAL
Labeler
Zydus Pharmaceuticals USA Inc.
Application
ANDA090697
Marketing category
ANDA
Marketing start
2017-12-05
Marketing end
0000-00-00
Substance
RAMIPRIL
Active strength
3 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68382-375-0168382037501100 TABLET in 1 BOTTLE (68382-375-01) 100 tablet2017-12-050000-00-00NoNoCurrent
68382-375-0568382037505500 TABLET in 1 BOTTLE (68382-375-05) 500 tablet2017-12-050000-00-00NoNoCurrent
68382-375-066838203750630 TABLET in 1 BOTTLE (68382-375-06) 30 tablet2017-12-050000-00-00NoNoCurrent
68382-375-10683820375101000 TABLET in 1 BOTTLE (68382-375-10) 1000 tablet2017-12-050000-00-00NoNoCurrent
68382-375-166838203751690 TABLET in 1 BOTTLE (68382-375-16) 90 tablet2017-12-050000-00-00NoNoCurrent
68382-375-776838203757710 BLISTER PACK in 1 CARTON (68382-375-77) > 10 TABLET in 1 BLISTER PACK10 blister pack2017-12-050000-00-00NoNoCurrent