NDC 71335-9701 – Hydromorphone Hydrochloride
Hydromorphone Hydrochloride 4 mg/1 · Tablet · Oral
Product NDC71335-9701
Product details
- Brand name
- Hydromorphone Hydrochloride
- Generic name
- Hydromorphone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA019892
- Marketed since
- November 23, 2009
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Hydromorphone Hydrochloride 4 mg/1
Uses, dosage, side effects and warnings for Hydromorphone Hydrochloride →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-9701-0 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-9701-0) | Feb 26, 2025 |
| 71335-9701-1 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-9701-1) | Jan 12, 2026 |
| 71335-9701-2 | 180 TABLET in 1 BOTTLE, PLASTIC (71335-9701-2) | Apr 10, 2026 |
| 71335-9701-3 | 120 TABLET in 1 BOTTLE, PLASTIC (71335-9701-3) | Apr 10, 2026 |
| 71335-9701-4 | 20 TABLET in 1 BOTTLE, PLASTIC (71335-9701-4) | Apr 10, 2026 |
| 71335-9701-5 | 25 TABLET in 1 BOTTLE, PLASTIC (71335-9701-5) | Apr 10, 2026 |
| 71335-9701-6 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-9701-6) | Apr 10, 2026 |
| 71335-9701-7 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-9701-7) | Jul 30, 2024 |
| 71335-9701-8 | 56 TABLET in 1 BOTTLE, PLASTIC (71335-9701-8) | Apr 10, 2026 |
| 71335-9701-9 | 140 TABLET in 1 BOTTLE, PLASTIC (71335-9701-9) | Apr 10, 2026 |
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