Cabergoline

Product NDC: 49884-673
11-digit product format: 498840673
Labeler code: 49884
Product ID: 49884-673_1c7edbc4-9a68-49b3-8ce6-67d25b6231d5
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Cabergoline
Dosage form: TABLET
Route: ORAL
Labeler: Par Pharmaceutical, Inc.
Application: ANDA076310
Marketing category: ANDA
Marketing start: 2005-12-29
Marketing end: 0000-00-00
Substance: CABERGOLINE
Active strength: 1 mg/1
Pharmacologic classes: Ergolines [CS],Ergot Derivative [EPC]
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
130aac29-e6c6-4d4b-17f4-126c01ca97cf	Product name	3	20250304

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49884-673-14	EA - Each	49884-673	78434a5d-f147-4a75-b6e3-1a732f7445bc	1	2012-07-24

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
199703	cabergoline 0.5 MG Oral Tablet	PSN	c85d676c-e23e-468d-9de3-79202d9fad3f	4
199703	cabergoline 0.5 MG Oral Tablet	SCD	c85d676c-e23e-468d-9de3-79202d9fad3f	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49884-673-14	49884067314	8 TABLET in 1 BOTTLE (49884-673-14)	8 tablet	2005-12-29	0000-00-00	No	No	Current