Thiothixene

Product NDC
70518-2544
11-digit product format
705182544
Labeler code
70518
Product ID
70518-2544_c9fef0fb-a467-d603-e053-2a95a90aec0e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Thiothixene
Dosage form
CAPSULE
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA211642
Marketing category
ANDA
Marketing start
2020-01-17
Marketing end
0000-00-00
Substance
THIOTHIXENE
Active strength
2 mg/1
Pharmacologic classes
Typical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70518-2544-02023-03-10C16284748780-1f386c649-f405-0266-e053-dadaa90a7c1a2385ed46-68ed-46ae-a809-d63a795ba28e
70518-2544-02023-01-30C16284748780-1f386c649-f405-0266-e053-dadaa90a7c1a2385ed46-68ed-46ae-a809-d63a795ba28e

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-2544-070518254400100 POUCH in 1 BOX (70518-2544-0) > 1 CAPSULE in 1 POUCH (70518-2544-1) 100 pouch2020-01-170000-00-00NoNoCurrent