Acid Controller

Product NDC
69842-267
11-digit product format
698420267
Labeler code
69842
Product ID
69842-267_a4abfc79-a092-fb3c-bb73-2e02326a614b
Type
HUMAN OTC DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET
Route
ORAL
Labeler
CVS Health Corp
Application
ANDA077367
Marketing category
ANDA
Marketing start
2020-10-01
Marketing end
0000-00-00
Substance
FAMOTIDINE
Active strength
20 mg/1
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-267ACID CONTROLLER ORIGINAL STRENGTH (FAMOTIDINE) TABLET ACID CONTROLLER MAXIMUM STRENGTH (FAMOTIDINE) TABLET [CVS HEALTH CORP]9Legacy NDC20241025_111a0385-0d44-d50e-28a6-54322138536b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-267-10698420267101 BOTTLE in 1 CARTON (69842-267-10) > 100 TABLET in 1 BOTTLE1 bottle2020-12-010000-00-00NoNoCurrent
69842-267-13698420267131 BOTTLE in 1 CARTON (69842-267-13) > 130 TABLET in 1 BOTTLE1 bottle2020-10-010000-00-00NoNoCurrent
69842-267-25698420267251 BOTTLE in 1 CARTON (69842-267-25) > 25 TABLET in 1 BOTTLE1 bottle2020-12-150000-00-00NoNoCurrent
69842-267-50698420267501 BOTTLE in 1 CARTON (69842-267-50) > 50 TABLET in 1 BOTTLE1 bottle2020-12-010000-00-00NoNoCurrent
69842-267-65698420267651 BOTTLE in 1 CARTON (69842-267-65) > 65 TABLET in 1 BOTTLE1 bottle2020-10-010000-00-00NoNoCurrent