NDC 76420-010 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 7.5 mg/1 · Tablet, Film Coated · Oral
Product NDC76420-010
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine Hydrochloride
- Labeler
- Asclemed USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078722
- Marketed since
- September 28, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Muscle Relaxant
Active ingredients
- Cyclobenzaprine Hydrochloride 7.5 mg/1
Uses, dosage, side effects and warnings for Cyclobenzaprine Hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 76420-010-01 | 100 TABLET, FILM COATED in 1 BOTTLE (76420-010-01) | Oct 21, 2022 |
| 76420-010-05 | 500 TABLET, FILM COATED in 1 BOTTLE (76420-010-05) | Oct 21, 2022 |
| 76420-010-12 | 120 TABLET, FILM COATED in 1 BOTTLE (76420-010-12) | Mar 16, 2023 |
| 76420-010-15 | 15 TABLET, FILM COATED in 1 BOTTLE (76420-010-15) | Oct 21, 2022 |
| 76420-010-30 | 30 TABLET, FILM COATED in 1 BOTTLE (76420-010-30) | Jan 23, 2020 |
| 76420-010-60 | 60 TABLET, FILM COATED in 1 BOTTLE (76420-010-60) | Jan 23, 2020 |
| 76420-010-90 | 90 TABLET, FILM COATED in 1 BOTTLE (76420-010-90) | Oct 21, 2022 |
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