dantrolene sodium
- Product NDC
- 42023-144
- 11-digit product format
- 420230144
- Labeler code
- 42023
- Product ID
- 42023-144_c89c6916-dcf1-46ee-bd91-4ee1245980c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dantrolene sodium
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- NDA017443
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2013-04-08
- Marketing end
- 2020-05-31
- Substance
- DANTROLENE SODIUM
- Active strength
- 25 mg/1
- Pharmacologic classes
- Decreased Striated Muscle Contraction [PE],Decreased Striated Muscle Tone [PE],Skeletal Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record