United States · FDA National Drug Code directory

Amitriptyline Hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
11788-077_4ee04ba3-df06-44c2-8476-09b6cd38f863
Product NDC
11788-077
Form
TABLET
Composition / generic term
Amitriptyline Hydrochloride
Labeler
AiPing Pharmaceutical, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20251101
Source listing expiry
20261231

Source-listed ingredients

  • AMITRIPTYLINE HYDROCHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (11788-077-01) · 11788-077-01
  • 1000 TABLET in 1 BOTTLE (11788-077-10) · 11788-077-10

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Amitriptyline Hydrochloride — United States | Molindra Medicines