NDC 71335-2341 – Dicyclomine Hydrochloride
Dicyclomine Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC71335-2341
Product details
- Brand name
- Dicyclomine Hydrochloride
- Generic name
- Dicyclomine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040317
- Marketed since
- April 25, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anticholinergic
Active ingredients
- Dicyclomine Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Dicyclomine Hydrochloride →
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2341-1 | 30 TABLET in 1 BOTTLE (71335-2341-1) | Feb 6, 2024 |
| 71335-2341-2 | 40 TABLET in 1 BOTTLE (71335-2341-2) | Feb 6, 2024 |
| 71335-2341-3 | 60 TABLET in 1 BOTTLE (71335-2341-3) | Feb 6, 2024 |
| 71335-2341-4 | 90 TABLET in 1 BOTTLE (71335-2341-4) | Feb 6, 2024 |
| 71335-2341-5 | 20 TABLET in 1 BOTTLE (71335-2341-5) | Feb 6, 2024 |
| 71335-2341-6 | 21 TABLET in 1 BOTTLE (71335-2341-6) | Feb 6, 2024 |
| 71335-2341-7 | 120 TABLET in 1 BOTTLE (71335-2341-7) | Feb 6, 2024 |
| 71335-2341-8 | 100 TABLET in 1 BOTTLE (71335-2341-8) | Feb 6, 2024 |
| 71335-2341-9 | 28 TABLET in 1 BOTTLE (71335-2341-9) | Feb 6, 2024 |
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