NDC 0185-0022 – Orphenadrine Citrate
Orphenadrine Citrate 100 mg/1 · Tablet, Extended Release · Oral
Product NDC0185-0022
Product details
- Brand name
- Orphenadrine Citrate
- Generic name
- Orphenadrine Citrate
- Labeler
- Sandoz Inc
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA040327
- Marketed since
- February 15, 2000
- Marketing end
- March 20, 2027
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Orphenadrine Citrate 100 mg/1
Uses, dosage, side effects and warnings for Orphenadrine citrate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0185-0022-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-0022-01) | Feb 15, 2000 |
Recalls mentioning this NDC
- D-0753-2022 Apr 13, 2022 · Class II
CGMP Deviations:Nitrosamine impurity (NMOA) above the acceptable daily limit. - D-1445-2014 Jul 30, 2014 · Class III
Failed Dissolution Specifications: Product found to be out of specification (OOS) during stability testing.
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