Methyldopa
- Product NDC
- 51079-201
- 11-digit product format
- 510790201
- Labeler code
- 51079
- Product ID
- 51079-201_96b15a17-a4b4-2f5c-e053-2a95a90a183f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methyldopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA070076
- Marketing category
- ANDA
- Marketing start
- 1998-09-01
- Marketing end
- 2020-02-29
- Substance
- METHYLDOPA
- Active strength
- 500 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