SERTRALINE HYDROCHLORIDE

Product NDC
55700-948
11-digit product format
557000948
Labeler code
55700
Product ID
55700-948_10f4f645-ae72-4bfd-ba49-bd662612f89e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
SERTRALINE HYDROCHLORIDE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Quality Care Products, LLC
Application
ANDA202825
Marketing category
ANDA
Marketing start
2021-09-27
Marketing end
0000-00-00
Substance
SERTRALINE HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Cytochrome P450 2D6 Inhibitors [MoA], Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-948-30EA - Each55700-9482b2beaf4-e769-42d7-8871-e19deabda45b12022-01-06
55700-948-90EA - Each55700-948b379a4f7-ce1b-4a97-87dc-606b610bbe6212021-11-09

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55700-948SERTRALINE HYDROCHLORIDE TABLET, FILM COATED [QUALITY CARE PRODUCTS, LLC]5Legacy NDC20241220_e6431b44-7a10-4c4f-a622-2f21207ff8e0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
55700-948-305570009483030 TABLET, FILM COATED in 1 BOTTLE (55700-948-30) 2021-11-220000-00-00NoNoCurrent
55700-948-905570009489090 TABLET, FILM COATED in 1 BOTTLE (55700-948-90) 2021-09-270000-00-00NoNoCurrent