Folic Acid
- Product NDC
- 50090-0200
- 11-digit product format
- 500900200
- Labeler code
- 50090
- Product ID
- 50090-0200_e5a8b37d-f804-47d2-9dbd-73050b910d13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040796
- Marketing category
- ANDA
- Marketing start
- 2009-06-01
- Marketing end
- 0000-00-00
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-0200-0 | EA - Each | 50090-0200 | 96beaa06-56f9-46bb-b997-7fec08d8c6d0 | 1 | 2018-08-13 |
| 50090-0200-2 | EA - Each | 50090-0200 | 13e3b6d5-18fa-4962-be20-2f162dfbb28b | 1 | 2018-08-13 |