NDC 47335-860 – Tramadol Hydrochloride
Tramadol Hydrochloride 200 mg/1 · Tablet, Extended Release · Oral
Product NDC47335-860
Product details
- Brand name
- Tramadol Hydrochloride
- Generic name
- Tramadol Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA201384
- Marketed since
- December 12, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Tramadol Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Tramadol Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 47335-860-08 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-08) | Dec 12, 2011 |
| 47335-860-18 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-18) | Dec 12, 2011 |
| 47335-860-83 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-83) | Dec 12, 2011 |
| 47335-860-88 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-88) | Dec 12, 2011 |
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