FOLIC ACID
- Product NDC
- 70518-0609
- 11-digit product format
- 705180609
- Labeler code
- 70518
- Product ID
- 70518-0609_e1fa9849-2908-ea02-e053-2995a90a1f1b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- folic acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204418
- Marketing category
- ANDA
- Marketing start
- 2017-07-06
- Marketing end
- 0000-00-00
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-0609-0 | 70518060900 | 50 TABLET in 1 BOTTLE, PLASTIC (70518-0609-0) | 50 tablet | 2017-07-06 | 0000-00-00 | No | No | Current |
| 70518-0609-1 | 70518060901 | 30 TABLET in 1 BLISTER PACK (70518-0609-1) | 30 tablet | 2017-12-12 | 0000-00-00 | No | No | Current |
| 70518-0609-2 | 70518060902 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-0609-2) | 100 tablet | 2018-05-14 | 0000-00-00 | No | No | Current |
| 70518-0609-3 | 70518060903 | 100 TABLET in 1 BOTTLE (70518-0609-3) | 100 tablet | 2020-06-26 | 0000-00-00 | No | No | Current |