NDC 72162-1359 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC72162-1359
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077797
- Marketed since
- March 30, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Cyclobenzaprine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1359-0 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-0) | Jan 31, 2024 |
| 72162-1359-1 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-1) | Jan 31, 2024 |
| 72162-1359-5 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1359-5) | Jan 31, 2024 |
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