NDC 72189-545 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC72189-545
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- Direct_Rx
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208170
- Marketed since
- April 9, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Cyclobenzaprine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 72189-545-15 | 15 TABLET, FILM COATED in 1 BOTTLE (72189-545-15) | Apr 9, 2024 |
| 72189-545-21 | 21 TABLET, FILM COATED in 1 BOTTLE (72189-545-21) | Apr 9, 2024 |
| 72189-545-30 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-545-30) | Apr 9, 2024 |
| 72189-545-60 | 60 TABLET, FILM COATED in 1 BOTTLE (72189-545-60) | Apr 9, 2024 |
| 72189-545-90 | 90 TABLET, FILM COATED in 1 BOTTLE (72189-545-90) | Apr 9, 2024 |
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