Aspire Night Cold and Flu Softgel
- Product NDC
- 81013-102
- 11-digit product format
- 810130102
- Labeler code
- 81013
- Product ID
- 81013-102_f1f406b0-c983-63ab-e053-2a95a90ad8c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aspire Night Cold and Flu Softgel
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Aspire Pharmaceuticals Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-03-17
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 325 mg/1; mg/1; mg/1; mg/1
- Pharmacologic classes
- Adrenergic alpha1-Agonists [MoA], Antihistamine [EPC], Histamine Receptor Antagonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81013-102-01 | 81013010201 | 5000 CAPSULE, LIQUID FILLED in 1 BAG (81013-102-01) | 2021-03-17 | 0000-00-00 | No | No | Current |