NDC 71335-2226 – Dicyclomine hydrochloride
Dicyclomine Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC71335-2226
Product details
- Brand name
- Dicyclomine hydrochloride
- Generic name
- Dicyclomine hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA216736
- Marketed since
- December 14, 2022
- 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 (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2226-0 | 10 TABLET in 1 BOTTLE (71335-2226-0) | Aug 23, 2023 |
| 71335-2226-1 | 30 TABLET in 1 BOTTLE (71335-2226-1) | Aug 23, 2023 |
| 71335-2226-2 | 40 TABLET in 1 BOTTLE (71335-2226-2) | Aug 23, 2023 |
| 71335-2226-3 | 60 TABLET in 1 BOTTLE (71335-2226-3) | Aug 23, 2023 |
| 71335-2226-4 | 90 TABLET in 1 BOTTLE (71335-2226-4) | Aug 23, 2023 |
| 71335-2226-5 | 20 TABLET in 1 BOTTLE (71335-2226-5) | Aug 23, 2023 |
| 71335-2226-6 | 21 TABLET in 1 BOTTLE (71335-2226-6) | Aug 23, 2023 |
| 71335-2226-7 | 120 TABLET in 1 BOTTLE (71335-2226-7) | Aug 23, 2023 |
| 71335-2226-8 | 100 TABLET in 1 BOTTLE (71335-2226-8) | Aug 23, 2023 |
| 71335-2226-9 | 28 TABLET in 1 BOTTLE (71335-2226-9) | Aug 23, 2023 |
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