Nifedipine

Product NDC
55154-0196
11-digit product format
551540196
Labeler code
55154
Product ID
55154-0196_472621b6-c2b7-4582-9ceb-7cead55ff247
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nifedipine
Dosage form
CAPSULE
Route
ORAL
Labeler
Cardinal Health 107, LLC
Application
ANDA202644
Marketing category
ANDA
Marketing start
2026-04-09
Substance
NIFEDIPINE
Active strength
10 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Nifedipine
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
NIFEDIPINE10 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiI9ZF7L6G2L
Rxcui198032

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bbd94e90-e531-9113-45c1-29860f331640Product name720230104
5e4d0a9b-8ce4-418c-bf0c-d2b4be281ffdProduct name420220126
308fd2ea-d88a-e021-96c1-7c2ab74d6e4bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55154-0196-0Nifedipine1 in 1 BLISTER PACKCAPSULE11
55154-0196-0Nifedipine10 in 1 BAGCAPSULE101

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198032NIFEdipine 10 MG Oral CapsulePSN472621b6-c2b7-4582-9ceb-7cead55ff2471
198032nifedipine 10 MG Oral CapsuleSCD472621b6-c2b7-4582-9ceb-7cead55ff2471

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
55154-0196-05515401960010 BLISTER PACK in 1 BAG (55154-0196-0) / 1 CAPSULE in 1 BLISTER PACK10 blister pack2026-04-09NoNoCurrent