Carbidopa

Product NDC: 43975-220
11-digit product format: 439750220
Labeler code: 43975
Product ID: 43975-220_4a568ee9-8920-46bf-9018-068a35d5c78b
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Carbidopa
Dosage form: TABLET
Route: ORAL
Labeler: ANI Pharmaceuticals, Inc.
Application: ANDA203261
Marketing category: ANDA
Marketing start: 2014-03-10
Marketing end: 2023-09-30
Substance: CARBIDOPA
Active strength: 25 mg/1
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
43975-220-10	EA - Each	43975-220	fbbbe9dd-9f21-44eb-aeeb-07183d937ac1	1	2014-04-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
43975-220-10	43975022010	100 TABLET in 1 BOTTLE (43975-220-10)	100 tablet	2014-03-10	0000-00-00	No	No	Current