NDC 71205-356 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-356
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208170
- Marketed since
- May 31, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71205-356-15 | 15 TABLET, FILM COATED in 1 BOTTLE (71205-356-15) | Jul 20, 2021 |
| 71205-356-20 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-356-20) | Apr 6, 2023 |
| 71205-356-21 | 21 TABLET, FILM COATED in 1 BOTTLE (71205-356-21) | Apr 6, 2023 |
| 71205-356-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-356-30) | Nov 1, 2019 |
| 71205-356-40 | 40 TABLET, FILM COATED in 1 BOTTLE (71205-356-40) | Jan 8, 2024 |
| 71205-356-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-356-60) | Nov 1, 2019 |
| 71205-356-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-356-90) | Nov 1, 2019 |
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