NDC 60760-767 – Cyclobenzaprine Hydrochloride
Cyclobenzaprine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC60760-767
Product details
- Brand name
- Cyclobenzaprine Hydrochloride
- Generic name
- Cyclobenzaprine hydrochloride
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208170
- Marketed since
- May 31, 2017
- 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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 60760-767-04 | 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-04) | Jun 20, 2023 |
| 60760-767-09 | 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-09) | Aug 10, 2023 |
| 60760-767-15 | 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-15) | Jun 8, 2023 |
| 60760-767-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-20) | Aug 1, 2023 |
| 60760-767-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-30) | Aug 1, 2023 |
| 60760-767-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-60) | May 18, 2026 |
| 60760-767-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-767-90) | Jul 7, 2023 |
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