Telmisartan

Product NDC
31722-803
11-digit product format
317220803
Labeler code
31722
Product ID
31722-803_95dc7a73-2c00-4e39-813a-a3f94f5e1b4b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Telmisartan
Dosage form
TABLET
Route
ORAL
Labeler
Camber Pharmaceuticals, Inc.
Application
ANDA205901
Marketing category
ANDA
Marketing start
2016-04-25
Marketing end
0000-00-00
Substance
TELMISARTAN
Active strength
40 mg/1
Pharmacologic classes
Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
31722-803-37EA - Each31722-803fe0dd0eb-4213-4574-94bd-a3356ea1980112017-09-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
31722-803-313172208033110 TABLET in 1 BLISTER PACK (31722-803-31) 10 tablet2016-04-250000-00-00NoNoCurrent
31722-803-323172208033215 TABLET in 1 CARTON (31722-803-32) 15 tablet2016-04-250000-00-00NoNoCurrent
31722-803-333172208033310 TABLET in 1 BLISTER PACK (31722-803-33) 10 tablet2016-04-250000-00-00NoNoCurrent
31722-803-343172208033415 TABLET in 1 CARTON (31722-803-34) 15 tablet2016-04-250000-00-00NoNoCurrent
31722-803-35317220803353 TABLET in 1 CARTON (31722-803-35) 3 tablet2016-04-250000-00-00NoNoCurrent
31722-803-363172208033610 TABLET in 1 BLISTER PACK (31722-803-36) 10 tablet2016-04-250000-00-00NoNoCurrent
31722-803-37317220803373 TABLET in 1 CARTON (31722-803-37) 3 tablet2016-04-250000-00-00NoNoCurrent