Tylo Night (Acetaminophen)
- Product NDC
- 49638-106
- Requested package NDC
- 49638-106-30
- 11-digit product format
- 496380106
- Labeler code
- 49638
- Product ID
- 49638-106_ca763b28-3c99-a5e5-e053-2995a90ab83c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- America Medic & Science, LLC
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-07-06
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 500 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49638-106 | TYLO NIGHT (ACETAMINOPHEN) (ACETAMINOPHEN) TABLET, DELAYED RELEASE [AMERICA MEDIC & SCIENCE, LLC] | 8 | Legacy NDC | 20240203_709babea-c67a-479b-b47e-18e935de5518.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49638-106-30 | 49638010630 | 1 BOTTLE in 1 CARTON (49638-106-30) > 30 TABLET, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2020-07-06 | 0000-00-00 | No | No | Current |