Metoprolol Succinate - ER Tablets 200 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

NDC 1167877-0593-30
Product NDC67877-0593
Generic Drug NameMetoprolol Succinate ER Tablets
Brand NameMetoprolol Succinate
ManufacturerAscend Laboratories, LLC
Strength200 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity30 Tablet, Film Coated, Extended Release
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-30)
Active IngredientsMetoprolol Succinate
Marketing CategoryANDA

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NDC snapshot

Metoprolol Succinate ER Tablets 200 mg / 1 Tablet is tracked under NDC 67877-0593-30 and rolls up into product family 67877-0593. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 30 Tablet, Film Coated, Extended Release.
  • Manufacturer: Ascend Laboratories, LLC.
  • Dosage form: Tablet.
  • Family size: 5 indexed presentations.

Official references

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

Alternate presentations in this family

These nearby package-level pages can help healthcare teams compare related packaging or presentation differences inside the same product-NDC family.

Metoprolol Succinate - ER Tablets 200 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release, NDC 67877-0593-30, is a Ascend Laboratories, LLC 200 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated, Extended Release.

NDC search formats

  • Canonical NDC 11: 67877-0593-30
  • Digits-only NDC 11: 67877059330
  • Possible 10-digit display format: 67877-593-30 (6787759330)

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