DermacinRx PureFolix
- Product NDC
- 59088-090
- 11-digit product format
- 590880090
- Labeler code
- 59088
- Product ID
- 59088-090_bec537b2-4f20-d94a-e053-2a95a90a61d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folic Acid, Vitamin D3
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-11-03
- Marketing end
- 2021-12-31
- Substance
- FOLIC ACID; VITAMIN D
- Active strength
- 1 mg/1; ug/1
- Pharmacologic classes
- Vitamin D [CS],Vitamin D [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 59088-090-54 | 59088009054 | 30 TABLET in 1 BOTTLE, PLASTIC (59088-090-54) | 30 tablet | 2015-11-03 | 0000-00-00 | No | No | Current |