Methyldopa
- Product NDC
- 68151-2791
- 11-digit product format
- 681512791
- Labeler code
- 68151
- Product ID
- 68151-2791_29a33fb6-f519-4c20-8dc4-c5286f79fbd2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methyldopa
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA070084
- Marketing category
- ANDA
- Marketing start
- 2012-07-24
- Marketing end
- 0000-00-00
- Substance
- METHYLDOPA
- Active strength
- 250 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-2791-5 | Methyldopa | 1 in 1 BOTTLE | TABLET, FILM COATED | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2791 | METHYLDOPA TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT] | 3 | Legacy NDC, 1 package rows | 20160213_e503c0bf-c326-48fb-8967-0f476eaa8961.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2791-5 | 68151279105 | 1 in 1 BOTTLE | Historical |