Folic Acid
- Product NDC
- 71335-0136
- 11-digit product format
- 713350136
- Labeler code
- 71335
- Product ID
- 71335-0136_0258c538-7511-4143-ab1a-f6446dde8c9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 |
|---|---|---|---|---|---|
| 71335-0136-1 | EA - Each | 71335-0136 | d1d95c22-8068-4b0e-a4ed-0b03a06c8a2b | 1 | 2018-03-08 |
| 71335-0136-2 | EA - Each | 71335-0136 | 1f739060-c2d5-4c5b-a813-d03ccaefbe43 | 1 | 2018-03-08 |
| 71335-0136-3 | EA - Each | 71335-0136 | 3eaddbd2-8648-4991-932d-376ff665b940 | 1 | 2018-03-08 |
| 71335-0136-4 | EA - Each | 71335-0136 | c506a6c3-c1cb-401d-9f1c-d0b2fd75a354 | 1 | 2018-03-08 |
| 71335-0136-5 | EA - Each | 71335-0136 | cd99e17d-6312-4579-9723-6610b1d8cd66 | 1 | 2018-03-08 |
| 71335-0136-6 | EA - Each | 71335-0136 | dcbf64e6-e471-4035-a8f0-e6a75351af1c | 1 | 2018-03-08 |