Methyldopa
- Product NDC
- 16729-030
- 11-digit product format
- 167290030
- Labeler code
- 16729
- Product ID
- 16729-030_baa618d9-f802-f827-e053-2995a90a09e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methyldopa
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Accord Healthcare Inc.
- Application
- ANDA070084
- Marketing category
- ANDA
- Marketing start
- 2012-07-24
- Marketing end
- 2022-08-31
- Substance
- METHYLDOPA
- Active strength
- 250 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16729-030-01 | 16729003001 | 100 TABLET, FILM COATED in 1 BOTTLE (16729-030-01) | 2012-07-24 | 2022-08-31 | No | No | Current |
| 16729-030-16 | 16729003016 | 500 TABLET, FILM COATED in 1 BOTTLE (16729-030-16) | 2013-01-21 | 2022-07-31 | No | No | Current |