Mexiletine hydrochloride 150 mg / 1 Capsule 30 Blister Pack

Reference details for licensed healthcare facility review and verification.

NDC 1160687-0778-21
Product NDC60687-0778
Generic Drug NameMexiletine hydrochloride
Brand NameMexiletine hydrochloride
ManufacturerAmerican Health Packaging
Strength150 mg / 1
Dosage FormCapsule
Drug TypeOral
Package Quantity30 Blister Pack
Package Description30 BLISTER PACK in 1 CARTON (60687-778-21) / 1 CAPSULE in 1 BLISTER PACK (60687-778-11)
Active IngredientsMexiletine Hydrochloride
Marketing CategoryANDA

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NDC snapshot

Mexiletine hydrochloride 150 mg / 1 Capsule is tracked under NDC 60687-0778-21 and rolls up into product family 60687-0778. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 30 Blister Pack.
  • Manufacturer: American Health Packaging.
  • Dosage form: Capsule.
  • 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.

Mexiletine hydrochloride 150 mg / 1 Capsule 30 Blister Pack, NDC 60687-0778-21, is a American Health Packaging 150 mg / 1 capsule presentation packaged as 30 Blister Pack.

NDC search formats

  • Canonical NDC 11: 60687-0778-21
  • Digits-only NDC 11: 60687077821
  • Possible 10-digit display format: 60687-778-21 (6068777821)

Helpful product links

  • Search by brand name: Mexiletine hydrochloride
  • NDC 11: 60687-0778-21
  • Product family NDC: 60687-0778
  • VA classification code: CV300
  • VA classification code description: ANTIARRHYTHMICS
  • CMOP ID: M0092
  • VUID: 4007667