ALERTNESS AID is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by We Care Distributor Inc.. The primary component is Caffeine.
Product ID | 70005-020_cc191c28-7fdf-41b0-8c30-46e358af0caa |
NDC | 70005-020 |
Product Type | Human Otc Drug |
Proprietary Name | ALERTNESS AID |
Generic Name | Caffeine Tablets, 200 Mg |
Dosage Form | Tablet, Coated |
Route of Administration | ORAL |
Marketing Start Date | 2016-03-07 |
Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
Application Number | part340 |
Labeler Name | We Care Distributor Inc. |
Substance Name | CAFFEINE |
Active Ingredient Strength | 200 mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2016-03-07 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph final |
Application Number | part340 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-03-07 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph final |
Application Number | part340 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-03-07 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph final |
Application Number | part340 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-03-07 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
CAFFEINE | 200 mg/1 |
SPL SET ID: | 7d671a58-ecb9-4368-8f7f-0b965e49cbcb |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
63940-229 | Alertness Aid | Caffeine |
68016-680 | Alertness Aid | Caffeine |
70000-0154 | Alertness Aid | Caffeine |
70005-020 | ALERTNESS AID | Caffeine Tablets, 200 mg |