Dantrium (Par Pharmaceutical, Inc.)
Welcome to the PulseAid listing for the Dantrium drug offered from Par Pharmaceutical, Inc.. This Decreased Striated Muscle Contraction [PE],Decreased Striated Muscle Tone [PE],Skeletal Muscle Relaxant [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Par Pharmaceutical, Inc. |
NON-PROPRIETARY NAME: | dantrolene sodium |
SUBSTANCE NAME: | DANTROLENE SODIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Decreased Striated Muscle Contraction [PE],Decreased Striated Muscle Tone [PE],Skeletal Muscle Relaxant [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2008-08-01 |
END MARKETING DATE: | 0000-00-00 |
Dantrium HUMAN PRESCRIPTION DRUG Details:
Item Description | Dantrium from Par Pharmaceutical, Inc. |
LABELER NAME: | Par Pharmaceutical, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 25(mg/1) |
START MARKETING DATE: | 2008-08-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 42023-124_a6e82749-6530-4e20-95a7-45bcd70aba3c |
PRODUCT NDC: | 42023-124 |
APPLICATION NUMBER: | NDA017443 |
Other DANTROLENE SODIUM Pharmaceutical Manufacturers / Labelers: