cyclobenzaprine hydrochloride
- Product NDC
- 0179-0057
- 11-digit product format
- 001790057
- Labeler code
- 0179
- Product ID
- 0179-0057_7b9a5b1c-afc4-12cc-e053-2a91aa0a07be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cyclobenzaprine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA077563
- Marketing category
- ANDA
- Marketing start
- 2010-03-02
- Marketing end
- 2020-02-29
- Substance
- CYCLOBENZAPRINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record