Folic Acid
- Product NDC
- 51079-105
- 11-digit product format
- 510790105
- Labeler code
- 51079
- Product ID
- 51079-105_7cd84a20-a032-43d9-e053-2a91aa0a84b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA040756
- Marketing category
- ANDA
- Marketing start
- 2011-04-21
- Marketing end
- 2019-07-31
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51079-105-01 | EA - Each | 51079-105 | c3552e62-0ef2-4dc2-afb4-3f946b232b17 | 1 | 2012-07-24 |
| 51079-105-17 | EA - Each | 51079-105 | 3834542a-4918-4956-b9bb-fc28b7ac74f0 | 1 | 2012-07-24 |
| 51079-105-19 | EA - Each | 51079-105 | dcfd24b5-88b4-4498-99e0-52937cebd395 | 1 | 2012-07-24 |
| 51079-105-20 | EA - Each | 51079-105 | ca2c7d96-c621-4e3d-87eb-1ff2047c848d | 1 | 2012-07-24 |