United States · FDA National Drug Code directory

DICYCLOMINE 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
72789-522_51043fad-02f3-b7fc-e063-6394a90a31f0
Product NDC
72789-522
Form
CAPSULE
Composition / generic term
DICYCLOMINE HYDROCHLORIDE
Labeler
PD-Rx Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20250930
Source listing expiry
20271231

Source-listed ingredients

  • DICYCLOMINE HYDROCHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE, PLASTIC (72789-522-01) · 72789-522-01
  • 20 CAPSULE in 1 BOTTLE, PLASTIC (72789-522-20) · 72789-522-20
  • 28 CAPSULE in 1 BOTTLE, PLASTIC (72789-522-28) · 72789-522-28
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-522-30) · 72789-522-30
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (72789-522-90) · 72789-522-90
  • 180 CAPSULE in 1 BOTTLE, PLASTIC (72789-522-93) · 72789-522-93
  • 1000 CAPSULE in 1 BOTTLE, PLASTIC (72789-522-95) · 72789-522-95
  • 120 CAPSULE in 1 BOTTLE, PLASTIC (72789-522-98) · 72789-522-98

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.

Browse United States records →