Metformin Hydrochloride NDC 71205-883

Product information

Brand name (proprietary)

Metformin Hydrochloride

Generic name (nonproprietary)

metformin hydrochloride

Active ingredients

Metformin hydrochloride — 850 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Proficient Rx LP

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 203769

Marketing start

Nov 21, 2017

Listing expires

Dec 31, 2026

Other FDA classes

Biguanides (Chemical structure)

Identifiers

Product ID 71205-883_27a10d92-3e03-4881-9b8f-7d0ee57cb744SPL ID 27a10d92-3e03-4881-9b8f-7d0ee57cb744SPL set ID 738402d6-3700-46b2-a90c-2e8f2c354a39RxCUI 861004, 861007, 861010UNII 786Z46389EUPC 0371205882723, 0371205883904, 0371205884604

Pharmacologic class

Biguanide

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471205088300 followed by a unit qualifier and the quantity Copy

Package 71205-0883-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 203769

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

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