Metformin Hydrochloride NDC 68788-8756

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

Preferred Pharmaceuticals Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 209882

Marketing start

Oct 14, 2024

Listing expires

Dec 31, 2027

Other FDA classes

Biguanides (Chemical structure)

Identifiers

Product ID 68788-8756_1bb1a8f7-db48-4add-9c43-c87a272c09f9SPL ID 1bb1a8f7-db48-4add-9c43-c87a272c09f9SPL set ID ca71c133-6c38-4b9e-80af-1949634157f4RxCUI 861010UNII 786Z46389E

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

N468788875601 followed by a unit qualifier and the quantity Copy

Package 68788-8756-01. 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

Other NDCs under ANDA 209882

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