Nimodipine

Product NDC
62559-210
Requested package NDC
62559-210-31
11-digit product format
625590210
Labeler code
62559
Product ID
62559-210_afe779b6-cc7b-42b0-87ba-a932477e170b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nimodipine
Dosage form
CAPSULE
Route
ORAL
Labeler
ANI Pharmaceuticals, Inc.
Application
ANDA201832
Marketing category
ANDA
Marketing start
2015-11-01
Marketing end
2022-09-30
Substance
NIMODIPINE
Active strength
30 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage62559-21062559-210-31DDiscontinued by firm2026-07-31

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A201832-001NIMODIPINENIMODIPINE30MGCAPSULE / ORAL2015-07-24

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-08-01 22:54:322026-06A201832-001NIMODIPINE30MGCAPSULE / ORAL2015-07-24a50c72e98297…

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62559-210-31EA - Each62559-2104e5cba1c-4f95-4a70-bb72-836af255caaf12016-01-13
62559-210-52EA - Each62559-210cc53fa8a-fc94-4f83-9617-d890ab9705af12016-01-13
62559-210-81EA - Each62559-2103ca74807-6290-4ff2-adb8-52bb2f9062f012016-01-13

DailyMed Socrata Ingredients#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62559-210-316255902103130 CAPSULE in 1 CARTON (62559-210-31) 30 capsule2015-11-010000-00-00NoNoCurrent