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
- 71335-0471_50d57cda-f389-4eed-a4e5-edec4388bb48
- Product NDC
- 71335-0471
- Form
- CAPSULE
- Composition / generic term
- Dicyclomine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19740930
- Source listing expiry
- 20271231
Source-listed ingredients
- DICYCLOMINE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (71335-0471-1) · 71335-0471-1
- 90 CAPSULE in 1 BOTTLE (71335-0471-2) · 71335-0471-2
- 40 CAPSULE in 1 BOTTLE (71335-0471-3) · 71335-0471-3
- 60 CAPSULE in 1 BOTTLE (71335-0471-4) · 71335-0471-4
- 20 CAPSULE in 1 BOTTLE (71335-0471-5) · 71335-0471-5
- 100 CAPSULE in 1 BOTTLE (71335-0471-6) · 71335-0471-6
- 180 CAPSULE in 1 BOTTLE (71335-0471-7) · 71335-0471-7
- 120 CAPSULE in 1 BOTTLE (71335-0471-8) · 71335-0471-8
- 10 CAPSULE in 1 BOTTLE (71335-0471-9) · 71335-0471-9
Source and coverage
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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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