Folic Acid
- Product NDC
- 71335-0760
- 11-digit product format
- 713350760
- Labeler code
- 71335
- Product ID
- 71335-0760_235fbac1-cc3f-43c5-be45-63447d6bddd9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091145
- Marketing category
- ANDA
- Marketing start
- 2015-03-01
- Marketing end
- 0000-00-00
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 71335-0760-1 | 71335076001 | 30 TABLET in 1 BOTTLE (71335-0760-1) | 30 tablet | 2016-03-11 | 0000-00-00 | No | No | Current |
| 71335-0760-2 | 71335076002 | 100 TABLET in 1 BOTTLE (71335-0760-2) | 100 tablet | 2016-03-11 | 0000-00-00 | No | No | Current |
| 71335-0760-3 | 71335076003 | 120 TABLET in 1 BOTTLE (71335-0760-3) | 120 tablet | 2016-03-11 | 0000-00-00 | No | No | Current |
| 71335-0760-4 | 71335076004 | 50 TABLET in 1 BOTTLE (71335-0760-4) | 50 tablet | 2016-03-11 | 0000-00-00 | No | No | Current |
| 71335-0760-5 | 71335076005 | 90 TABLET in 1 BOTTLE (71335-0760-5) | 90 tablet | 2016-03-11 | 0000-00-00 | No | No | Current |
| 71335-0760-6 | 71335076006 | 60 TABLET in 1 BOTTLE (71335-0760-6) | 60 tablet | 2016-03-11 | 0000-00-00 | No | No | Current |
| 71335-0760-7 | 71335076007 | 10 TABLET in 1 BOTTLE (71335-0760-7) | 10 tablet | 2016-03-11 | 0000-00-00 | No | No | Current |