Midodrine Hydrochloride
- Product NDC
- 63739-145
- 11-digit product format
- 637390145
- Labeler code
- 63739
- Product ID
- 63739-145_e82fa2f0-d741-1fa8-e053-2995a90a2ec3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- midodrine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation DBA SKY Packaging
- Application
- ANDA207849
- Marketing category
- ANDA
- Marketing start
- 2020-10-15
- Marketing end
- 0000-00-00
- Substance
- MIDODRINE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-145 | MIDODRINE HYDROCHLORIDE TABLET [MCKESSON CORPORATION DBA SKY PACKAGING] | 10 | Legacy NDC | 20250112_e81e4324-8264-9ee6-e053-2995a90a8673.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-145-10 | 63739014510 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-145-10) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2022-09-08 | 0000-00-00 | No | No | Current |