Temazepam

Product NDC
70518-3227
11-digit product format
705183227
Labeler code
70518
Product ID
70518-3227_ccc026f6-98ae-c6f5-e053-2a95a90ac261
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Temazepam
Dosage form
CAPSULE
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA203482
Marketing category
ANDA
Marketing start
2021-09-23
Marketing end
0000-00-00
Substance
TEMAZEPAM
Active strength
30 mg/1
Pharmacologic classes
Benzodiazepine [EPC],Benzodiazepines [CS]
DEA schedule
CIV
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
70518-3227-02023-03-22C16284748780-1f386c649-9a56-0266-e053-dadaa90a7c1a95274e13-e1d4-4896-a43a-812ddfe38406
70518-3227-02023-01-30C16284748780-1f386c649-9a56-0266-e053-dadaa90a7c1a95274e13-e1d4-4896-a43a-812ddfe38406

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-3227-070518322700100 POUCH in 1 BOX (70518-3227-0) > 1 CAPSULE in 1 POUCH (70518-3227-1) 100 pouch2021-09-230000-00-00NoNoCurrent