| Product NDC: | 11528-095 |
| Proprietary Name: | Paire OB Plus DHA |
| Non Proprietary Name: | Paire OB Plus DHA |
| Active Ingredient(s): | & nbsp; Paire OB Plus DHA |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11528-095 |
| Labeler Name: | Centrix Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101013 |
| Package NDC: | 11528-095-03 |
| Package Description: | 1 KIT in 1 CARTON (11528-095-03) * 5 TABLET in 1 BLISTER PACK * 5 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
| NDC Code | 11528-095-03 |
| Proprietary Name | Paire OB Plus DHA |
| Package Description | 1 KIT in 1 CARTON (11528-095-03) * 5 TABLET in 1 BLISTER PACK * 5 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
| Product NDC | 11528-095 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Paire OB Plus DHA |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20101013 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Centrix Pharmaceutical, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |