Amantadine HCl

Product NDC
71335-0279
11-digit product format
713350279
Labeler code
71335
Product ID
71335-0279_c0ba2d5b-b2e4-4ffc-b166-4bf369b292bb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
AMANTADINE HYDROCHLORIDE
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078720
Marketing category
ANDA
Marketing start
2016-08-15
Marketing end
0000-00-00
Substance
AMANTADINE HYDROCHLORIDE
Active strength
100 mg/1
Pharmacologic classes
Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-0279-17133502790120 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0279-1) 2017-03-240000-00-00NoNoCurrent
71335-0279-27133502790230 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0279-2) 2017-03-240000-00-00NoNoCurrent
71335-0279-37133502790310 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0279-3) 2017-03-240000-00-00NoNoCurrent
71335-0279-47133502790414 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0279-4) 2017-03-240000-00-00NoNoCurrent
71335-0279-57133502790560 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-0279-5) 2017-03-240000-00-00NoNoCurrent