Betaine Anhydrous
- Product NDC
- 70954-331
- 11-digit product format
- 709540331
- Labeler code
- 70954
- Product ID
- 70954-331_dd16eeb4-3f4f-4381-a395-54c32ab6e4df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betaine Anhydrous
- Dosage form
- FOR SOLUTION
- Route
- ORAL
- Labeler
- Novitium Pharma LLC
- Application
- ANDA214864
- Marketing category
- ANDA
- Marketing start
- 2021-11-23
- Marketing end
- 0000-00-00
- Substance
- BETAINE
- Active strength
- 1 g/g
- Pharmacologic classes
- Methylating Activity [MoA],Methylating Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70954-331-10 | 70954033110 | 180 g in 1 BOTTLE (70954-331-10) | 180 g | 2021-11-23 | 0000-00-00 | No | No | Current |