Cyclobenzaprine Hydrochloride
- Product NDC
- 63739-531
- 11-digit product format
- 637390531
- Labeler code
- 63739
- Product ID
- 63739-531_b3c7fd07-1923-498c-e053-2a95a90a02ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cyclobenzaprine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA077797
- Marketing category
- ANDA
- Marketing start
- 2007-02-28
- Marketing end
- 2021-07-31
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-531-10 | 63739053110 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-531-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2007-02-28 | 2021-07-31 | No | No | Current |