Carvedilol
- Product NDC
- 55700-819
- 11-digit product format
- 557000819
- Labeler code
- 55700
- Product ID
- 55700-819_38008a81-8df6-47c1-bac4-eddacbc08edf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carvedilol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA078384
- Marketing category
- ANDA
- Marketing start
- 2019-11-14
- Marketing end
- 0000-00-00
- Substance
- CARVEDILOL
- Active strength
- 6 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA],Adrenergic beta1-Antagonists [MoA],Adrenergic beta2-Antagonists [MoA],alpha-Adrenergic Blocker [EPC],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-819-18 | 55700081918 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-819-18) | 2019-11-14 | 0000-00-00 | No | No | Current |
| 55700-819-90 | 55700081990 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-819-90) | 2020-02-14 | 0000-00-00 | No | No | Current |