extra strength pain relief
Generic: acetaminophen
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
extra strength pain relief
Generic Name
acetaminophen
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-1516
Product ID
63629-1516_86dfb73f-2bff-4d40-accd-422643f7358b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
1989-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636291516
Hyphenated Format
63629-1516
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
extra strength pain relief (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 250 TABLET in 1 BOTTLE (63629-1516-0)
- 20 TABLET in 1 BOTTLE (63629-1516-1)
- 15 TABLET in 1 BOTTLE (63629-1516-2)
- 40 TABLET in 1 BOTTLE (63629-1516-3)
- 100 TABLET in 1 BOTTLE (63629-1516-4)
- 30 TABLET in 1 BOTTLE (63629-1516-5)
- 45 TABLET in 1 BOTTLE (63629-1516-6)
- 50 TABLET in 1 BOTTLE (63629-1516-7)
- 60 TABLET in 1 BOTTLE (63629-1516-8)
- 90 TABLET in 1 BOTTLE (63629-1516-9)
Packages (10)
63629-1516-0
250 TABLET in 1 BOTTLE (63629-1516-0)
63629-1516-1
20 TABLET in 1 BOTTLE (63629-1516-1)
63629-1516-2
15 TABLET in 1 BOTTLE (63629-1516-2)
63629-1516-3
40 TABLET in 1 BOTTLE (63629-1516-3)
63629-1516-4
100 TABLET in 1 BOTTLE (63629-1516-4)
63629-1516-5
30 TABLET in 1 BOTTLE (63629-1516-5)
63629-1516-6
45 TABLET in 1 BOTTLE (63629-1516-6)
63629-1516-7
50 TABLET in 1 BOTTLE (63629-1516-7)
63629-1516-8
60 TABLET in 1 BOTTLE (63629-1516-8)
63629-1516-9
90 TABLET in 1 BOTTLE (63629-1516-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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