Bimatoprost

Product NDC
50383-908
11-digit product format
503830908
Labeler code
50383
Product ID
50383-908_9e7758d0-19d9-4ee1-86ad-f068a5c98e9d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Bimatoprost
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Akorn
Application
ANDA203299
Marketing category
ANDA
Marketing start
2018-11-12
Marketing end
0000-00-00
Substance
BIMATOPROST
Active strength
0 mg/mL
Pharmacologic classes
Prostaglandin Analog [EPC], Prostaglandins [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f71952f0-5c3a-ff37-f1fb-fed3868f6302Product name820260105
546f403c-5466-48b9-a79e-80b68d2b77d8Product name120200706
3471d048-4165-432e-a2dc-905eb43247dbProduct name420200611

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50383-908BIMATOPROST SOLUTION/ DROPS [AKORN]9Legacy NDC20220308_ce5c7f22-ade3-41ea-8dd8-3ec0399d3279.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50383-908-02503830908021 BOTTLE, DROPPER in 1 CARTON (50383-908-02) > 2.5 mL in 1 BOTTLE, DROPPER2018-11-120000-00-00NoNoCurrent
50383-908-05503830908051 BOTTLE, DROPPER in 1 CARTON (50383-908-05) > 5 mL in 1 BOTTLE, DROPPER2018-11-120000-00-00NoNoCurrent
50383-908-07503830908071 BOTTLE, DROPPER in 1 CARTON (50383-908-07) > 7.5 mL in 1 BOTTLE, DROPPER2018-11-120000-00-00NoNoCurrent