Carbidopa and Levodopa

Product NDC: 63739-108
11-digit product format: 637390108
Labeler code: 63739
Product ID: 63739-108_b4923de8-9bc5-3626-e053-2a95a90ab1e3
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Carbidopa and Levodopa
Dosage form: TABLET
Route: ORAL
Labeler: McKesson Corporation dba SKY Packaging
Application: ANDA073589
Marketing category: ANDA
Marketing start: 2018-07-16
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
63739-108-10	2020-07-22	C162847	48780-1	ab0e2407-35d8-f274-e053-dbdaa90a6471	a9d3e19b-8536-4618-badb-ce314427151c

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63739-108-10	EA - Each	63739-108	9ffc200b-f0cc-4d73-9ed1-e7bef307ff6e	1	2019-11-12

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63739-108-10	63739010810	10 BLISTER PACK in 1 BOX (63739-108-10) > 10 TABLET in 1 BLISTER PACK	10 blister pack	2019-10-01	0000-00-00	No	No	Current