Metformin Hydrochloride 850 mg / 1 Tablet 30 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

NDC 1170882-0125-30
Product NDC70882-0125
Generic Drug NameMetformin Hydrochloride
Brand NameMetformin Hydrochloride
ManufacturerCambridge Therapeutics Technologies, LLC
Strength850 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity30 Tablet, Film Coated
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70882-125-30)
Active IngredientsMetformin Hydrochloride
Marketing CategoryANDA

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NDC snapshot

Metformin Hydrochloride 850 mg / 1 Tablet is tracked under NDC 70882-0125-30 and rolls up into product family 70882-0125. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 30 Tablet, Film Coated.
  • Manufacturer: Cambridge Therapeutics Technologies, LLC.
  • Dosage form: Tablet.
  • Family size: 1 indexed presentation.

Official references

Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.

Potential alternatives with matching presentation

Open the comparison hub or review package-level listings from 2 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.

View Potential Alternative HubMetformin Hydrochloride 850 mg / 1 Tablet 30 Tablet, Film Coated Blister2 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Metformin Hydrochloride 850 mg / 1 Tablet 30 Tablet, Film Coated, NDC 70882-0125-30, is a Cambridge Therapeutics Technologies, LLC 850 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated.

NDC search formats

  • Canonical NDC 11: 70882-0125-30
  • Digits-only NDC 11: 70882012530
  • Possible 10-digit display format: 70882-125-30 (7088212530)

Helpful product links

  • Search by brand name: Metformin Hydrochloride
  • NDC 11: 70882-0125-30
  • Product family NDC: 70882-0125
  • VA classification code: HS502
  • VA classification code description: ORAL HYPOGLYCEMIC AGENTS,ORAL
  • CMOP ID: M0263
  • VUID: 4012736