Bromocriptine Mesylate

Product NDC
60687-931
11-digit product format
606870931
Labeler code
60687
Product ID
60687-931_51911920-109b-a9be-e063-6394a90a733f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Bromocriptine Mesylate
Dosage form
TABLET
Route
ORAL
Labeler
American Health Packaging
Application
NDA017962
Marketing category
NDA
Marketing start
2026-05-01
Substance
BROMOCRIPTINE MESYLATE
Active strength
2.5 mg/1
Pharmacologic classes
Ergolines [CS], Ergot Derivative [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BROMOCRIPTINE MESYLATE2.5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiFFP983J3OD

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
90f4f2b3-d032-9eaf-93c5-f165b5a4c90eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60687-931-11Bromocriptine Mesylate1 in 1 BLISTER PACKTABLET11
60687-931-21Bromocriptine Mesylate30 in 1 CARTONTABLET301

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197411bromocriptine mesylate 2.5 MG Oral TabletPSNddd292a5-72af-448f-8b88-cc4fd99ec7831
197411bromocriptine 2.5 MG Oral TabletSCDddd292a5-72af-448f-8b88-cc4fd99ec7831
197411bromocriptine (as bromocriptine mesylate) 2.5 MG Oral TabletSYddd292a5-72af-448f-8b88-cc4fd99ec7831

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
60687-931-11606870931111 in 1 BLISTER PACKHistorical
60687-931-216068709312130 BLISTER PACK in 1 CARTON (60687-931-21) / 1 TABLET in 1 BLISTER PACK (60687-931-11) 30 blister pack2026-05-01NoNoCurrent