Carbidopa and levodopa

Product NDC: 63739-017
11-digit product format: 637390017
Labeler code: 63739
Product ID: 63739-017_cfe3d82e-1df9-41d9-ba0b-d8759172292a
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Carbidopa and levodopa
Dosage form: TABLET
Route: ORAL
Labeler: McKesson Corporation dba SKY Packaging
Application: ANDA074260
Marketing category: ANDA
Marketing start: 2016-07-18
Marketing end: 0000-00-00
Substance: CARBIDOPA; LEVODOPA
Active strength: 25 mg/1; mg/1
Pharmacologic classes: Aromatic Amino Acid [EPC],Amino Acids, Aromatic [CS]
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63739-017-10	2020-07-22	C162847	48780-1	ab0e2407-2747-f274-e053-dbdaa90a6471	c7724398-c494-4c66-8d50-672bde9446aa

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63739-017-10	EA - Each	63739-017	e218cb70-3f30-4bc5-835f-5d4e16d62f98	1	2017-08-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63739-017-10	63739001710	10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-017-10) > 10 TABLET in 1 BLISTER PACK	10 blister pack	2017-06-28	0000-00-00	No	No	Current