Betaine Anhydrous for Oral Solution
- Product NDC
- 72647-900
- 11-digit product format
- 726470900
- Labeler code
- 72647
- Product ID
- 72647-900_acce10dd-c8fa-4457-b3ed-d716c9978e29
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betaine Anhydrous
- Dosage form
- FOR SOLUTION
- Route
- ORAL
- Labeler
- OAKRUM PHARMA, LLC
- Application
- ANDA214864
- Marketing category
- ANDA
- Marketing start
- 2022-02-03
- Marketing end
- 2024-04-30
- Substance
- BETAINE
- Active strength
- 1 g/g
- Pharmacologic classes
- Methylating Activity [MoA], Methylating Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 72647-900-01 | 72647090001 | 180 g in 1 BOTTLE (72647-900-01) | 180 g | 2022-02-03 | 0000-00-00 | No | No | Current |