METFORMIN HYDROCHLORIDE

Product NDC: 55700-730
11-digit product format: 557000730
Labeler code: 55700
Product ID: 55700-730_3dd815dc-7484-4663-bf39-ea4e49e53883
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: METFORMIN HYDROCHLORIDE
Dosage form: TABLET
Route: ORAL
Labeler: Quality Care Products, LLC
Application: ANDA203769
Marketing category: ANDA
Marketing start: 2019-03-15
Marketing end: 0000-00-00
Substance: METFORMIN HYDROCHLORIDE
Active strength: 850 mg/1
Pharmacologic classes: Biguanide [EPC],Biguanides [CS]
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55700-730-90	2025-01-10	C162847	48780-1	f386c649-9c3b-0266-e053-dadaa90a7c1a	ffa799e3-d749-41df-a8af-e01cd53172b6
55700-730-90	2023-01-30	C162847	48780-1	f386c649-9c3b-0266-e053-dadaa90a7c1a	ffa799e3-d749-41df-a8af-e01cd53172b6

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
55700-730-90	EA - Each	55700-730	b42b90b3-5f01-48b9-9b7d-1387abeb13e0	1	2019-04-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
55700-730-90	55700073090	90 TABLET in 1 BOTTLE, PLASTIC (55700-730-90)	90 tablet	2019-03-15	0000-00-00	No	No	Current